GET https://dev.normadoc.fr/_partial/cart/summary?template=%40SyliusShop%2FCart%2F_widget.html.twig

Response
200 OK
IP
216.73.217.87
Profiled on
Token
73dfa4

Components

5 Twig Components
47 Render Count
95 ms Render Time
162.0 MiB Memory Usage

Components

Name Metadata Render Count Render Time
ProductCard 
"App\Twig\Components\ProductCard"
components/ProductCard.html.twig 		15 90.11ms
ProductState 
"App\Twig\Components\ProductState"
components/ProductState.html.twig 		15 2.29ms
ProductMostRecent 
"App\Twig\Components\ProductMostRecent"
components/ProductMostRecent.html.twig 		15 9.00ms
PageBanner 
"App\Twig\Components\PageBanner"
components/PageBanner.html.twig 		1 4.57ms
BackButton 
"App\Twig\Components\BackButton"
components/BackButton.html.twig 		1 0.22ms

Render calls

PageBanner App\Twig\Components\PageBanner 162.0 MiB 4.57 ms
Input props 
[
  "backLabel" => "33.100 : Electromagnetic compatibility (EMC)"
  "backUrl" => "/taxons/main/ics-2277/33-telecommunications-audio-and-video-engineering-4436/33-100-electromagnetic-compatibility-emc-4456"
  "paddingClasses" => "p-2 px-lg-5 py-lg-0"
  "searchPlaceholder" => "sylius.ui.search"
  "showSearch" => "true"
  "title" => "33.100.20 : Immunity"
]
Attributes 
[]
Component 
App\Twig\Components\PageBanner {#94284
  +supTitle: null
  +title: "33.100.20 : Immunity"
  +subTitle: null
  +backUrl: "/taxons/main/ics-2277/33-telecommunications-audio-and-video-engineering-4436/33-100-electromagnetic-compatibility-emc-4456"
  +backLabel: "33.100 : Electromagnetic compatibility (EMC)"
  +customClasses: null
  +backgroundType: null
  +centered: true
  +showSearch: true
  +searchPlaceholder: "sylius.ui.search"
  +searchValue: null
  +paddingClasses: "p-2 px-lg-5 py-lg-0"
}
BackButton App\Twig\Components\BackButton 162.0 MiB 0.22 ms
Input props 
[
  "url" => "/taxons/main/ics-2277/33-telecommunications-audio-and-video-engineering-4436/33-100-electromagnetic-compatibility-emc-4456"
  "label" => "33.100 : Electromagnetic compatibility (EMC)"
]
Attributes 
[]
Component 
App\Twig\Components\BackButton {#94386
  +label: "33.100 : Electromagnetic compatibility (EMC)"
  +url: "/taxons/main/ics-2277/33-telecommunications-audio-and-video-engineering-4436/33-100-electromagnetic-compatibility-emc-4456"
}
ProductCard App\Twig\Components\ProductCard 162.0 MiB 9.47 ms
Input props 
[
  "product" => App\Entity\Product\Product {#94933
    #id: 8398
    #code: "IEEE00000408"
    #attributes: Doctrine\ORM\PersistentCollection {#94994 …}
    #variants: Doctrine\ORM\PersistentCollection {#94992 …}
    #options: Doctrine\ORM\PersistentCollection {#94988 …}
    #associations: Doctrine\ORM\PersistentCollection {#94990 …}
    #createdAt: DateTime @1751037383 {#94930
      date: 2025-06-27 17:16:23.0 Europe/Paris (+02:00)
    }
    #updatedAt: DateTime @1754606304 {#94936
      date: 2025-08-08 00:38:24.0 Europe/Paris (+02:00)
    }
    #enabled: true
    #translations: Doctrine\ORM\PersistentCollection {#95004 …}
    #translationsCache: [
      "en_US" => App\Entity\Product\ProductTranslation {#95527
        #locale: "en_US"
        #translatable: App\Entity\Product\Product {#94933}
        #id: 28601
        #name: "IEEE 213:1987 (R1998)"
        #slug: "ieee-213-1987-r1998-ieee00000408-240050"
        #description: """
          Revision Standard - Inactive-Withdrawn.<br />\n
          Procedures for testing television and FM broadcast receivers are included. The user is cautioned that this method might not be appropriate for conducted emissions testing of systems or products other than televisions or FM receivers. Other more general methods exist and it is suggested that they be used for review. These include, but are not limited to, ANSI C63.4-1981, American National Standard Methods of Measurement of Radio Noise Emissions from Low-Voltage Electrical and Electronic Equipment in the Range of 10 kHz to 1 GHz. A method for measuring the emissions conducted by the power line from these receivers in the frequency range of 300 kHz to 25 MHz is defined. Standard input signals, the equipment setup, and measurement techniques are described.<br />\n
          \t\t\t\t
          """
        #metaKeywords: null
        #metaDescription: null
        #shortDescription: "IEEE Standard Procedure for Measuring Conducted Emissions in the Range of 300 kHz to 25 MHz from Television and FM Broadcast Receivers to Power Lines"
        -notes: "Inactive-Withdrawn"
      }
    ]
    #currentLocale: "en_US"
    #currentTranslation: null
    #fallbackLocale: "en_US"
    #variantSelectionMethod: "match"
    #productTaxons: Doctrine\ORM\PersistentCollection {#95002 …}
    #channels: Doctrine\ORM\PersistentCollection {#94996 …}
    #mainTaxon: App\Entity\Taxonomy\Taxon {#8840 …}
    #reviews: Doctrine\ORM\PersistentCollection {#95000 …}
    #averageRating: 0.0
    #images: Doctrine\ORM\PersistentCollection {#94998 …}
    -supplier: Proxies\__CG__\App\Entity\Supplier\Supplier {#95011 …}
    -subscriptionCollections: Doctrine\ORM\PersistentCollection {#95010 …}
    -apiLastModifiedAt: DateTime @1754517600 {#94941
      date: 2025-08-07 00:00:00.0 Europe/Paris (+02:00)
    }
    -lastUpdatedAt: DateTime @1578006000 {#94944
      date: 2020-01-03 00:00:00.0 Europe/Paris (+01:00)
    }
    -author: ""
    -publishedAt: DateTime @588981600 {#94942
      date: 1988-08-31 00:00:00.0 Europe/Paris (+02:00)
    }
    -releasedAt: null
    -confirmedAt: DateTime @898725600 {#94940
      date: 1998-06-25 00:00:00.0 Europe/Paris (+02:00)
    }
    -canceledAt: DateTime @1074207600 {#94939
      date: 2004-01-16 00:00:00.0 Europe/Paris (+01:00)
    }
    -edition: null
    -coreDocument: "213"
    -bookCollection: ""
    -pageCount: 23
    -documents: Doctrine\ORM\PersistentCollection {#95008 …}
    -favorites: Doctrine\ORM\PersistentCollection {#95006 …}
  }
  "layout" => "vertical"
  "showPrice" => true
  "showStatusBadges" => true
  "imageFilter" => "product_listing_thumbnail"
  "additionalClasses" => "h-100 border-0"
  "hasStretchedLink" => true
  "backgroundColor" => "white"
  "hoverType" => "border-black"
]
Attributes 
[]
Component 
App\Twig\Components\ProductCard {#95411
  +product: App\Entity\Product\Product {#94933
    #id: 8398
    #code: "IEEE00000408"
    #attributes: Doctrine\ORM\PersistentCollection {#94994 …}
    #variants: Doctrine\ORM\PersistentCollection {#94992 …}
    #options: Doctrine\ORM\PersistentCollection {#94988 …}
    #associations: Doctrine\ORM\PersistentCollection {#94990 …}
    #createdAt: DateTime @1751037383 {#94930
      date: 2025-06-27 17:16:23.0 Europe/Paris (+02:00)
    }
    #updatedAt: DateTime @1754606304 {#94936
      date: 2025-08-08 00:38:24.0 Europe/Paris (+02:00)
    }
    #enabled: true
    #translations: Doctrine\ORM\PersistentCollection {#95004 …}
    #translationsCache: [
      "en_US" => App\Entity\Product\ProductTranslation {#95527
        #locale: "en_US"
        #translatable: App\Entity\Product\Product {#94933}
        #id: 28601
        #name: "IEEE 213:1987 (R1998)"
        #slug: "ieee-213-1987-r1998-ieee00000408-240050"
        #description: """
          Revision Standard - Inactive-Withdrawn.<br />\n
          Procedures for testing television and FM broadcast receivers are included. The user is cautioned that this method might not be appropriate for conducted emissions testing of systems or products other than televisions or FM receivers. Other more general methods exist and it is suggested that they be used for review. These include, but are not limited to, ANSI C63.4-1981, American National Standard Methods of Measurement of Radio Noise Emissions from Low-Voltage Electrical and Electronic Equipment in the Range of 10 kHz to 1 GHz. A method for measuring the emissions conducted by the power line from these receivers in the frequency range of 300 kHz to 25 MHz is defined. Standard input signals, the equipment setup, and measurement techniques are described.<br />\n
          \t\t\t\t
          """
        #metaKeywords: null
        #metaDescription: null
        #shortDescription: "IEEE Standard Procedure for Measuring Conducted Emissions in the Range of 300 kHz to 25 MHz from Television and FM Broadcast Receivers to Power Lines"
        -notes: "Inactive-Withdrawn"
      }
    ]
    #currentLocale: "en_US"
    #currentTranslation: null
    #fallbackLocale: "en_US"
    #variantSelectionMethod: "match"
    #productTaxons: Doctrine\ORM\PersistentCollection {#95002 …}
    #channels: Doctrine\ORM\PersistentCollection {#94996 …}
    #mainTaxon: App\Entity\Taxonomy\Taxon {#8840 …}
    #reviews: Doctrine\ORM\PersistentCollection {#95000 …}
    #averageRating: 0.0
    #images: Doctrine\ORM\PersistentCollection {#94998 …}
    -supplier: Proxies\__CG__\App\Entity\Supplier\Supplier {#95011 …}
    -subscriptionCollections: Doctrine\ORM\PersistentCollection {#95010 …}
    -apiLastModifiedAt: DateTime @1754517600 {#94941
      date: 2025-08-07 00:00:00.0 Europe/Paris (+02:00)
    }
    -lastUpdatedAt: DateTime @1578006000 {#94944
      date: 2020-01-03 00:00:00.0 Europe/Paris (+01:00)
    }
    -author: ""
    -publishedAt: DateTime @588981600 {#94942
      date: 1988-08-31 00:00:00.0 Europe/Paris (+02:00)
    }
    -releasedAt: null
    -confirmedAt: DateTime @898725600 {#94940
      date: 1998-06-25 00:00:00.0 Europe/Paris (+02:00)
    }
    -canceledAt: DateTime @1074207600 {#94939
      date: 2004-01-16 00:00:00.0 Europe/Paris (+01:00)
    }
    -edition: null
    -coreDocument: "213"
    -bookCollection: ""
    -pageCount: 23
    -documents: Doctrine\ORM\PersistentCollection {#95008 …}
    -favorites: Doctrine\ORM\PersistentCollection {#95006 …}
  }
  +layout: "vertical"
  +showPrice: true
  +showStatusBadges: true
  +additionalClasses: "h-100 border-0"
  +linkLabel: ""
  +imageFilter: "product_listing_thumbnail"
  +hasStretchedLink: true
  +backgroundColor: "white"
  +hoverType: "border-black"
}
ProductState App\Twig\Components\ProductState 162.0 MiB 0.20 ms
Input props 
[
  "product" => App\Entity\Product\Product {#94933
    #id: 8398
    #code: "IEEE00000408"
    #attributes: Doctrine\ORM\PersistentCollection {#94994 …}
    #variants: Doctrine\ORM\PersistentCollection {#94992 …}
    #options: Doctrine\ORM\PersistentCollection {#94988 …}
    #associations: Doctrine\ORM\PersistentCollection {#94990 …}
    #createdAt: DateTime @1751037383 {#94930
      date: 2025-06-27 17:16:23.0 Europe/Paris (+02:00)
    }
    #updatedAt: DateTime @1754606304 {#94936
      date: 2025-08-08 00:38:24.0 Europe/Paris (+02:00)
    }
    #enabled: true
    #translations: Doctrine\ORM\PersistentCollection {#95004 …}
    #translationsCache: [
      "en_US" => App\Entity\Product\ProductTranslation {#95527
        #locale: "en_US"
        #translatable: App\Entity\Product\Product {#94933}
        #id: 28601
        #name: "IEEE 213:1987 (R1998)"
        #slug: "ieee-213-1987-r1998-ieee00000408-240050"
        #description: """
          Revision Standard - Inactive-Withdrawn.<br />\n
          Procedures for testing television and FM broadcast receivers are included. The user is cautioned that this method might not be appropriate for conducted emissions testing of systems or products other than televisions or FM receivers. Other more general methods exist and it is suggested that they be used for review. These include, but are not limited to, ANSI C63.4-1981, American National Standard Methods of Measurement of Radio Noise Emissions from Low-Voltage Electrical and Electronic Equipment in the Range of 10 kHz to 1 GHz. A method for measuring the emissions conducted by the power line from these receivers in the frequency range of 300 kHz to 25 MHz is defined. Standard input signals, the equipment setup, and measurement techniques are described.<br />\n
          \t\t\t\t
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        #metaKeywords: null
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        -notes: "Inactive-Withdrawn"
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    #currentLocale: "en_US"
    #currentTranslation: null
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    #variantSelectionMethod: "match"
    #productTaxons: Doctrine\ORM\PersistentCollection {#95002 …}
    #channels: Doctrine\ORM\PersistentCollection {#94996 …}
    #mainTaxon: App\Entity\Taxonomy\Taxon {#8840 …}
    #reviews: Doctrine\ORM\PersistentCollection {#95000 …}
    #averageRating: 0.0
    #images: Doctrine\ORM\PersistentCollection {#94998 …}
    -supplier: Proxies\__CG__\App\Entity\Supplier\Supplier {#95011 …}
    -subscriptionCollections: Doctrine\ORM\PersistentCollection {#95010 …}
    -apiLastModifiedAt: DateTime @1754517600 {#94941
      date: 2025-08-07 00:00:00.0 Europe/Paris (+02:00)
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    -lastUpdatedAt: DateTime @1578006000 {#94944
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    -author: ""
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      date: 1988-08-31 00:00:00.0 Europe/Paris (+02:00)
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    }
    -edition: null
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    -bookCollection: ""
    -pageCount: 23
    -documents: Doctrine\ORM\PersistentCollection {#95008 …}
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]
Attributes 
[
  "showFullLabel" => false
]
Component 
App\Twig\Components\ProductState {#95534
  +product: App\Entity\Product\Product {#94933
    #id: 8398
    #code: "IEEE00000408"
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          Revision Standard - Inactive-Withdrawn.<br />\n
          Procedures for testing television and FM broadcast receivers are included. The user is cautioned that this method might not be appropriate for conducted emissions testing of systems or products other than televisions or FM receivers. Other more general methods exist and it is suggested that they be used for review. These include, but are not limited to, ANSI C63.4-1981, American National Standard Methods of Measurement of Radio Noise Emissions from Low-Voltage Electrical and Electronic Equipment in the Range of 10 kHz to 1 GHz. A method for measuring the emissions conducted by the power line from these receivers in the frequency range of 300 kHz to 25 MHz is defined. Standard input signals, the equipment setup, and measurement techniques are described.<br />\n
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        #metaKeywords: null
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    #currentLocale: "en_US"
    #currentTranslation: null
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    #averageRating: 0.0
    #images: Doctrine\ORM\PersistentCollection {#94998 …}
    -supplier: Proxies\__CG__\App\Entity\Supplier\Supplier {#95011 …}
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    -apiLastModifiedAt: DateTime @1754517600 {#94941
      date: 2025-08-07 00:00:00.0 Europe/Paris (+02:00)
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    -lastUpdatedAt: DateTime @1578006000 {#94944
      date: 2020-01-03 00:00:00.0 Europe/Paris (+01:00)
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    -author: ""
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      date: 1988-08-31 00:00:00.0 Europe/Paris (+02:00)
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    -releasedAt: null
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      date: 1998-06-25 00:00:00.0 Europe/Paris (+02:00)
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      date: 2004-01-16 00:00:00.0 Europe/Paris (+01:00)
    }
    -edition: null
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    -pageCount: 23
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  }
  +appearance: "state-withdrawn"
  +labels: [
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  -stateAttributeCode: "state"
  -localeContext: Sylius\Component\Locale\Context\CompositeLocaleContext {#1833 …}
}
ProductMostRecent App\Twig\Components\ProductMostRecent 162.0 MiB 0.66 ms
Input props 
[
  "product" => App\Entity\Product\Product {#94933
    #id: 8398
    #code: "IEEE00000408"
    #attributes: Doctrine\ORM\PersistentCollection {#94994 …}
    #variants: Doctrine\ORM\PersistentCollection {#94992 …}
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      date: 2025-06-27 17:16:23.0 Europe/Paris (+02:00)
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      date: 2025-08-08 00:38:24.0 Europe/Paris (+02:00)
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    #enabled: true
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          Revision Standard - Inactive-Withdrawn.<br />\n
          Procedures for testing television and FM broadcast receivers are included. The user is cautioned that this method might not be appropriate for conducted emissions testing of systems or products other than televisions or FM receivers. Other more general methods exist and it is suggested that they be used for review. These include, but are not limited to, ANSI C63.4-1981, American National Standard Methods of Measurement of Radio Noise Emissions from Low-Voltage Electrical and Electronic Equipment in the Range of 10 kHz to 1 GHz. A method for measuring the emissions conducted by the power line from these receivers in the frequency range of 300 kHz to 25 MHz is defined. Standard input signals, the equipment setup, and measurement techniques are described.<br />\n
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]
Attributes 
[]
Component 
App\Twig\Components\ProductMostRecent {#95628
  +product: App\Entity\Product\Product {#94933
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        #description: """
          Revision Standard - Inactive-Withdrawn.<br />\n
          Procedures for testing television and FM broadcast receivers are included. The user is cautioned that this method might not be appropriate for conducted emissions testing of systems or products other than televisions or FM receivers. Other more general methods exist and it is suggested that they be used for review. These include, but are not limited to, ANSI C63.4-1981, American National Standard Methods of Measurement of Radio Noise Emissions from Low-Voltage Electrical and Electronic Equipment in the Range of 10 kHz to 1 GHz. A method for measuring the emissions conducted by the power line from these receivers in the frequency range of 300 kHz to 25 MHz is defined. Standard input signals, the equipment setup, and measurement techniques are described.<br />\n
          \t\t\t\t
          """
        #metaKeywords: null
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    #currentLocale: "en_US"
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ProductMostRecent App\Twig\Components\ProductMostRecent 162.0 MiB 0.58 ms
Input props 
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ProductCard App\Twig\Components\ProductCard 162.0 MiB 5.39 ms
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ProductCard App\Twig\Components\ProductCard 162.0 MiB 5.17 ms
Input props 
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          This recommended practice is intended to serve as a guide for health-care organizations in evaluating the radiated radio-frequency (RF) electromagnetic immunity of their existing inventories of medical devices to their existing inventories of RF transmitters, as well as to RF transmitters that are commonly available. It can also be used for newly purchased medical devices and RF transmitters, as well as for prepurchase evaluation.<br />\n
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          This recommended practice is intended to serve as a guide for health-care organizations in evaluating the radiated radio-frequency (RF) electromagnetic immunity of their existing inventories of medical devices to their existing inventories of RF transmitters, as well as to RF transmitters that are commonly available. It can also be used for newly purchased medical devices and RF transmitters, as well as for prepurchase evaluation.<br />\n
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Input props 
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          This recommended practice is intended to serve as a guide for health-care organizations in evaluating the radiated radio-frequency (RF) electromagnetic immunity of their existing inventories of medical devices to their existing inventories of RF transmitters, as well as to RF transmitters that are commonly available. It can also be used for newly purchased medical devices and RF transmitters, as well as for prepurchase evaluation.<br />\n
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          New IEEE Standard - Inactive-Withdrawn.<br />\n
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ProductMostRecent App\Twig\Components\ProductMostRecent 162.0 MiB 0.56 ms
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App\Twig\Components\ProductMostRecent {#96990
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          Guidance is provided for health-care organizations in evaluating the radiated RF electromagnetic immunity of their existing inventories of medical devices to their existing inventories of RF transmitters, as well as to RF transmitters that are commonly available. This recommended practice can also be used for newly purchased medical devices and RF transmitters, as well as for pre-purchase evaluation. It applies to medical devices used in health-care facilities and to portable transmitters with a rated power output of 8 W or less. It does not apply to implantable medical devices, transport environments such as ambulances and helicopters, or to RF transmitters rated at more than 8 W.<br />\n
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          The purpose of this recommended practice is to a) Provide an inexpensive, relatively reproducible test method for estimating the radiated RF electromagnetic immunity of medical devices to available, portable RF transmitters that might be operated in proximity; b) Provide a test method that can be performed by clinical and biomedical engineers;c) Improve reproducibility and intercomparability of test results; and d) Provide information for and facilitate development of policies and procedures for managing (i.e., allowing or restricting) the use of specific RF transmitters within specific areas of a health-care facility.
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Component 
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          \t\t\t\t<br />\n
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Component 
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ProductMostRecent App\Twig\Components\ProductMostRecent 162.0 MiB 0.56 ms
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          This immunity measurement and measurement instrumentation specification document complements the recommended procedures for making emission measurements as specified in ANSI C63.4. The immunity methods are alternative methods that might be of use to manufacturers who want to ensure a reliable product and reduce customer complaints by adding some additional immunity into their products beyond that required by law or by correcting problems experienced in the field not related to regulatory requirements. This document generally covers the frequency range of 30 Hz to 10 GHz.<br />\n
          \t\t\t\t<br />\n
          The conducted immunity (CI) and radiated immunity (RI) test methods in this recommended practice do not universally apply to every product. Applicable test methods should be selected. A qualified EMC engineer should document test planning and the rationale for using particular immunity tests. This document is intended to Identify preferred or optional immunity test methods.Describe specific measurement techniques.Suggest product performance degradation criteria as applicable to general and specific products.Identify test instrumentation specifications. Wherever possible, existing voluntary standards are utilized and summarized. It should be noted that the techniques listed herein should in no way limit the user to a particular method to increase product immunity. The immunity levels in this document are recommended. Should product classifications and type have other immunity levels that apply, they shall take precedence. Equipment developed for military applications should use MIL-STD-461E or later editions for test procedures and limits.
          """
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        #metaDescription: null
        #shortDescription: "American National Standard Recommended Practice for the Immunity Measurement of Electrical and Electronic Equipment"
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ProductCard App\Twig\Components\ProductCard 162.0 MiB 6.20 ms
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        #slug: "ieee-ansi-c63-18-2014-ieee00005407-242646"
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          Revision Standard - Active.<br />\n
          A guide to evaluating electromagnetic immunity of medical devices against radiated radio-frequency (RF) emissions from common RF transmitters is provided in this recommended practice (e.g., two-way radios; walkie-talkies; mobile phones; wireless-enabled tablets, e-readers, laptop computers, and similar devices; RFID readers; networked mp3 players; two-way pagers; and wireless personal digital assistants [PDAs]). A comprehensive test or a guarantee is not provided by this protocol but, instead, a basic evaluation is given that can help identify medical devices that might be particularly vulnerable to interference from common RF transmitters. Existing or newly purchased medical devices can be evaluated by this ad hoc test protocol or the protocol can be implemented for prepurchase evaluation. This recommended practice applies to medical devices used in health-care facilities but can also be adapted to medical devices in home health-care or mobile health-care settings. It does not apply to implantable medical devices (e.g., pacemakers and defibrillators), transport environments such as ambulances and helicopters, or RF transmitters rated at more than 8 W of output power. Testing with transmitters greater than 8 W in health-care facilities is not recommended because of possible adverse effects on critical care medical devices that are in use in nearby areas of the facility. Finally, in-band RF interference where the fundamental frequency of an RF transmitter overlaps with frequencies used by a hospital wireless network or monitoring or other medical device wireless links is not addressed by this recommended practice.<br />\n
          \t\t\t\t<br />\n
          This recommended practice is a guide to evaluating the electromagnetic immunity of medical devices to radiated radio-frequency (RF) emissions from common RF transmitters (e.g., two-way radios; walkie-talkies; mobile phones; wireless-enabled tablets, e-readers, laptop computers, and similar devices; radio-frequency identification (RFID) readers; networked mp3 players; two-way pagers; and wireless personal digital assistants [PDAs]). This protocol does not provide a comprehensive test or offer any guarantee, but it is a basic evaluation that can help identify medical devices that might be particularly vulnerable to interference from common RF transmitters. The ad hoc test protocol can be used to evaluate existing or newly purchased medical devices or can be implemented for the purpose of prepurchase evaluation. This recommended practice applies to medical devices used in health-care facilities, but it can also be adapted to medical devices in home health-care or mobile health-care settings. It does not apply to implantable medical devices (e.g., pacemakers and defibrillators), transport environments such as ambulances and helicopters, or RF transmitters rated at more than 8 W of output power. Testing with transmitters greater than 8 W in health-care facilities is not recommended because of possible adverse effects on critical-care medical devices that are in use in nearby areas of the facility. Finally, this recommended practice does not address in-band RF interference where the fundamental frequency of an RF transmitter overlaps with frequencies used by a hospital wireless network or monitoring or used by other medical device wireless links.<br />\n
          The purpose of this recommended practice is to provide an ad hoc test method to estimate the electromagnetic immunity of medical devices and help identify interference issues that might exist with critical medical devices as a result of emissions from RF transmitters increasingly used in health-care facilities, particularly by doctors, staff, patients, and visitors. RF transmitters include two-way radios, walkie-talkies, mobile phones, wireless-enabled laptop computers and similar devices,1 RFID readers, networked mp3 players, two-way pagers, wireless PDAs, and wireless medical devices. The test protocol is designed to be performed as follows:<br />\n
          a) By clinical engineers, biomedical engineers, and other technical personnel<br />\n
          b) In a way that is relatively rapid and practical<br />\n
          c) In an area and with equipment that are commonly available<br />\n
          d) To identify specific effects and thresholds (i.e., transmit power and distance) to provide the basic information needed to develop a mitigation action plan<br />\n
          e) To generate test results that can be used in the formulation of policies and procedures for managing the use of RF transmitters within a health-care facility<br />\n
          A preferred method (5.6.2) and several alternative RF sources and methods (Annex C) for ad hoc testing are outlined in this recommended practice to allow flexibility with regard to the time, personnel, and resources available to perform the testing. As a result, these different options provide different levels of accuracy and comprehensiveness. The most appropriate ad hoc test strategy will depend on the needs and resources of the user of this recommended practice. This recommended practice also provides guidance for selection of the medical devices to be tested, operation of RF transmitters used as RF test sources, and assessment of test results.<br />\n
          The preferred method for evaluation in most circumstances involves the use of the actual RF transmitter(s) (e.g., mobile phones and portable and mobile radios) as test sources to generate the same RF signals that would be encountered in the health-care facility. This approach also assumes that the end user has limited time and resources, a small number of critical medical devices to test, a limited space in which to perform the testing, and a single or a small number of specific RF transmitter signals to examine. In this preferred method, the RF transmitter is placed in a constantly transmitting state (i.e., test mode). The tests can be performed with or without an electric-field-strength (E-field) meter, although the use of an E-field meter is recommended.<br />\n
          Anotherre important function of this recommended practice is to define a consistent test protocol to allow results to be obtained and compared within and across institutions. Clinical and biomedical engineers have performed their own rudimentary (“ad hoc”) electromagnetic compatibility (EMC) testing using in-house methodology, RF transmitter sources, and medical devices. As a result, a comparison of the findings between health-care organizations might not be appropriate. To facilitate a comparison between health-care organizations, it is important that the recommendations herein are followed, deviations are kept to a minimum, and the testing is performed as consistently as possible.<br />\n
          Policies and procedures for mitigation of electromagnetic interference (EMI)^2 in health-care facilities, including the use or restriction of specific RF transmitters within specific areas, often called an exclusion zone, should be based on objective information, including that obtained by the use of this test method. A common problem with exclusion zones is that they are difficult to enforce, particularly with the increasingly common use of wireless devices and their expanding variety of applications, including use in medical equipment. With regard to purchase evaluation, confirming that medical devices conform to voluntary EMC immunity standards can provide some information, although many RF transmitters are able to exceed these immunity levels greatly when held close to a medical device. This recommended practice can be used to supplement the information obtained by testing for conformance to voluntary EMC standards. A list of EMC standards and guidelines that contain radiated RF immunity requirements applicable to medical devices as well as additional background information and further recommendations for mitigation of EMI in health-care facilities are presented in the annexes.
          """
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Component 
App\Twig\Components\ProductCard {#98190
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          Revision Standard - Active.<br />\n
          A guide to evaluating electromagnetic immunity of medical devices against radiated radio-frequency (RF) emissions from common RF transmitters is provided in this recommended practice (e.g., two-way radios; walkie-talkies; mobile phones; wireless-enabled tablets, e-readers, laptop computers, and similar devices; RFID readers; networked mp3 players; two-way pagers; and wireless personal digital assistants [PDAs]). A comprehensive test or a guarantee is not provided by this protocol but, instead, a basic evaluation is given that can help identify medical devices that might be particularly vulnerable to interference from common RF transmitters. Existing or newly purchased medical devices can be evaluated by this ad hoc test protocol or the protocol can be implemented for prepurchase evaluation. This recommended practice applies to medical devices used in health-care facilities but can also be adapted to medical devices in home health-care or mobile health-care settings. It does not apply to implantable medical devices (e.g., pacemakers and defibrillators), transport environments such as ambulances and helicopters, or RF transmitters rated at more than 8 W of output power. Testing with transmitters greater than 8 W in health-care facilities is not recommended because of possible adverse effects on critical care medical devices that are in use in nearby areas of the facility. Finally, in-band RF interference where the fundamental frequency of an RF transmitter overlaps with frequencies used by a hospital wireless network or monitoring or other medical device wireless links is not addressed by this recommended practice.<br />\n
          \t\t\t\t<br />\n
          This recommended practice is a guide to evaluating the electromagnetic immunity of medical devices to radiated radio-frequency (RF) emissions from common RF transmitters (e.g., two-way radios; walkie-talkies; mobile phones; wireless-enabled tablets, e-readers, laptop computers, and similar devices; radio-frequency identification (RFID) readers; networked mp3 players; two-way pagers; and wireless personal digital assistants [PDAs]). This protocol does not provide a comprehensive test or offer any guarantee, but it is a basic evaluation that can help identify medical devices that might be particularly vulnerable to interference from common RF transmitters. The ad hoc test protocol can be used to evaluate existing or newly purchased medical devices or can be implemented for the purpose of prepurchase evaluation. This recommended practice applies to medical devices used in health-care facilities, but it can also be adapted to medical devices in home health-care or mobile health-care settings. It does not apply to implantable medical devices (e.g., pacemakers and defibrillators), transport environments such as ambulances and helicopters, or RF transmitters rated at more than 8 W of output power. Testing with transmitters greater than 8 W in health-care facilities is not recommended because of possible adverse effects on critical-care medical devices that are in use in nearby areas of the facility. Finally, this recommended practice does not address in-band RF interference where the fundamental frequency of an RF transmitter overlaps with frequencies used by a hospital wireless network or monitoring or used by other medical device wireless links.<br />\n
          The purpose of this recommended practice is to provide an ad hoc test method to estimate the electromagnetic immunity of medical devices and help identify interference issues that might exist with critical medical devices as a result of emissions from RF transmitters increasingly used in health-care facilities, particularly by doctors, staff, patients, and visitors. RF transmitters include two-way radios, walkie-talkies, mobile phones, wireless-enabled laptop computers and similar devices,1 RFID readers, networked mp3 players, two-way pagers, wireless PDAs, and wireless medical devices. The test protocol is designed to be performed as follows:<br />\n
          a) By clinical engineers, biomedical engineers, and other technical personnel<br />\n
          b) In a way that is relatively rapid and practical<br />\n
          c) In an area and with equipment that are commonly available<br />\n
          d) To identify specific effects and thresholds (i.e., transmit power and distance) to provide the basic information needed to develop a mitigation action plan<br />\n
          e) To generate test results that can be used in the formulation of policies and procedures for managing the use of RF transmitters within a health-care facility<br />\n
          A preferred method (5.6.2) and several alternative RF sources and methods (Annex C) for ad hoc testing are outlined in this recommended practice to allow flexibility with regard to the time, personnel, and resources available to perform the testing. As a result, these different options provide different levels of accuracy and comprehensiveness. The most appropriate ad hoc test strategy will depend on the needs and resources of the user of this recommended practice. This recommended practice also provides guidance for selection of the medical devices to be tested, operation of RF transmitters used as RF test sources, and assessment of test results.<br />\n
          The preferred method for evaluation in most circumstances involves the use of the actual RF transmitter(s) (e.g., mobile phones and portable and mobile radios) as test sources to generate the same RF signals that would be encountered in the health-care facility. This approach also assumes that the end user has limited time and resources, a small number of critical medical devices to test, a limited space in which to perform the testing, and a single or a small number of specific RF transmitter signals to examine. In this preferred method, the RF transmitter is placed in a constantly transmitting state (i.e., test mode). The tests can be performed with or without an electric-field-strength (E-field) meter, although the use of an E-field meter is recommended.<br />\n
          Anotherre important function of this recommended practice is to define a consistent test protocol to allow results to be obtained and compared within and across institutions. Clinical and biomedical engineers have performed their own rudimentary (“ad hoc”) electromagnetic compatibility (EMC) testing using in-house methodology, RF transmitter sources, and medical devices. As a result, a comparison of the findings between health-care organizations might not be appropriate. To facilitate a comparison between health-care organizations, it is important that the recommendations herein are followed, deviations are kept to a minimum, and the testing is performed as consistently as possible.<br />\n
          Policies and procedures for mitigation of electromagnetic interference (EMI)^2 in health-care facilities, including the use or restriction of specific RF transmitters within specific areas, often called an exclusion zone, should be based on objective information, including that obtained by the use of this test method. A common problem with exclusion zones is that they are difficult to enforce, particularly with the increasingly common use of wireless devices and their expanding variety of applications, including use in medical equipment. With regard to purchase evaluation, confirming that medical devices conform to voluntary EMC immunity standards can provide some information, although many RF transmitters are able to exceed these immunity levels greatly when held close to a medical device. This recommended practice can be used to supplement the information obtained by testing for conformance to voluntary EMC standards. A list of EMC standards and guidelines that contain radiated RF immunity requirements applicable to medical devices as well as additional background information and further recommendations for mitigation of EMI in health-care facilities are presented in the annexes.
          """
        #metaKeywords: null
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ProductState App\Twig\Components\ProductState 162.0 MiB 0.15 ms
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        #description: """
          Revision Standard - Active.<br />\n
          A guide to evaluating electromagnetic immunity of medical devices against radiated radio-frequency (RF) emissions from common RF transmitters is provided in this recommended practice (e.g., two-way radios; walkie-talkies; mobile phones; wireless-enabled tablets, e-readers, laptop computers, and similar devices; RFID readers; networked mp3 players; two-way pagers; and wireless personal digital assistants [PDAs]). A comprehensive test or a guarantee is not provided by this protocol but, instead, a basic evaluation is given that can help identify medical devices that might be particularly vulnerable to interference from common RF transmitters. Existing or newly purchased medical devices can be evaluated by this ad hoc test protocol or the protocol can be implemented for prepurchase evaluation. This recommended practice applies to medical devices used in health-care facilities but can also be adapted to medical devices in home health-care or mobile health-care settings. It does not apply to implantable medical devices (e.g., pacemakers and defibrillators), transport environments such as ambulances and helicopters, or RF transmitters rated at more than 8 W of output power. Testing with transmitters greater than 8 W in health-care facilities is not recommended because of possible adverse effects on critical care medical devices that are in use in nearby areas of the facility. Finally, in-band RF interference where the fundamental frequency of an RF transmitter overlaps with frequencies used by a hospital wireless network or monitoring or other medical device wireless links is not addressed by this recommended practice.<br />\n
          \t\t\t\t<br />\n
          This recommended practice is a guide to evaluating the electromagnetic immunity of medical devices to radiated radio-frequency (RF) emissions from common RF transmitters (e.g., two-way radios; walkie-talkies; mobile phones; wireless-enabled tablets, e-readers, laptop computers, and similar devices; radio-frequency identification (RFID) readers; networked mp3 players; two-way pagers; and wireless personal digital assistants [PDAs]). This protocol does not provide a comprehensive test or offer any guarantee, but it is a basic evaluation that can help identify medical devices that might be particularly vulnerable to interference from common RF transmitters. The ad hoc test protocol can be used to evaluate existing or newly purchased medical devices or can be implemented for the purpose of prepurchase evaluation. This recommended practice applies to medical devices used in health-care facilities, but it can also be adapted to medical devices in home health-care or mobile health-care settings. It does not apply to implantable medical devices (e.g., pacemakers and defibrillators), transport environments such as ambulances and helicopters, or RF transmitters rated at more than 8 W of output power. Testing with transmitters greater than 8 W in health-care facilities is not recommended because of possible adverse effects on critical-care medical devices that are in use in nearby areas of the facility. Finally, this recommended practice does not address in-band RF interference where the fundamental frequency of an RF transmitter overlaps with frequencies used by a hospital wireless network or monitoring or used by other medical device wireless links.<br />\n
          The purpose of this recommended practice is to provide an ad hoc test method to estimate the electromagnetic immunity of medical devices and help identify interference issues that might exist with critical medical devices as a result of emissions from RF transmitters increasingly used in health-care facilities, particularly by doctors, staff, patients, and visitors. RF transmitters include two-way radios, walkie-talkies, mobile phones, wireless-enabled laptop computers and similar devices,1 RFID readers, networked mp3 players, two-way pagers, wireless PDAs, and wireless medical devices. The test protocol is designed to be performed as follows:<br />\n
          a) By clinical engineers, biomedical engineers, and other technical personnel<br />\n
          b) In a way that is relatively rapid and practical<br />\n
          c) In an area and with equipment that are commonly available<br />\n
          d) To identify specific effects and thresholds (i.e., transmit power and distance) to provide the basic information needed to develop a mitigation action plan<br />\n
          e) To generate test results that can be used in the formulation of policies and procedures for managing the use of RF transmitters within a health-care facility<br />\n
          A preferred method (5.6.2) and several alternative RF sources and methods (Annex C) for ad hoc testing are outlined in this recommended practice to allow flexibility with regard to the time, personnel, and resources available to perform the testing. As a result, these different options provide different levels of accuracy and comprehensiveness. The most appropriate ad hoc test strategy will depend on the needs and resources of the user of this recommended practice. This recommended practice also provides guidance for selection of the medical devices to be tested, operation of RF transmitters used as RF test sources, and assessment of test results.<br />\n
          The preferred method for evaluation in most circumstances involves the use of the actual RF transmitter(s) (e.g., mobile phones and portable and mobile radios) as test sources to generate the same RF signals that would be encountered in the health-care facility. This approach also assumes that the end user has limited time and resources, a small number of critical medical devices to test, a limited space in which to perform the testing, and a single or a small number of specific RF transmitter signals to examine. In this preferred method, the RF transmitter is placed in a constantly transmitting state (i.e., test mode). The tests can be performed with or without an electric-field-strength (E-field) meter, although the use of an E-field meter is recommended.<br />\n
          Anotherre important function of this recommended practice is to define a consistent test protocol to allow results to be obtained and compared within and across institutions. Clinical and biomedical engineers have performed their own rudimentary (“ad hoc”) electromagnetic compatibility (EMC) testing using in-house methodology, RF transmitter sources, and medical devices. As a result, a comparison of the findings between health-care organizations might not be appropriate. To facilitate a comparison between health-care organizations, it is important that the recommendations herein are followed, deviations are kept to a minimum, and the testing is performed as consistently as possible.<br />\n
          Policies and procedures for mitigation of electromagnetic interference (EMI)^2 in health-care facilities, including the use or restriction of specific RF transmitters within specific areas, often called an exclusion zone, should be based on objective information, including that obtained by the use of this test method. A common problem with exclusion zones is that they are difficult to enforce, particularly with the increasingly common use of wireless devices and their expanding variety of applications, including use in medical equipment. With regard to purchase evaluation, confirming that medical devices conform to voluntary EMC immunity standards can provide some information, although many RF transmitters are able to exceed these immunity levels greatly when held close to a medical device. This recommended practice can be used to supplement the information obtained by testing for conformance to voluntary EMC standards. A list of EMC standards and guidelines that contain radiated RF immunity requirements applicable to medical devices as well as additional background information and further recommendations for mitigation of EMI in health-care facilities are presented in the annexes.
          """
        #metaKeywords: null
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          \t\t\t\t<br />\n
          This recommended practice is a guide to evaluating the electromagnetic immunity of medical devices to radiated radio-frequency (RF) emissions from common RF transmitters (e.g., two-way radios; walkie-talkies; mobile phones; wireless-enabled tablets, e-readers, laptop computers, and similar devices; radio-frequency identification (RFID) readers; networked mp3 players; two-way pagers; and wireless personal digital assistants [PDAs]). This protocol does not provide a comprehensive test or offer any guarantee, but it is a basic evaluation that can help identify medical devices that might be particularly vulnerable to interference from common RF transmitters. The ad hoc test protocol can be used to evaluate existing or newly purchased medical devices or can be implemented for the purpose of prepurchase evaluation. This recommended practice applies to medical devices used in health-care facilities, but it can also be adapted to medical devices in home health-care or mobile health-care settings. It does not apply to implantable medical devices (e.g., pacemakers and defibrillators), transport environments such as ambulances and helicopters, or RF transmitters rated at more than 8 W of output power. Testing with transmitters greater than 8 W in health-care facilities is not recommended because of possible adverse effects on critical-care medical devices that are in use in nearby areas of the facility. Finally, this recommended practice does not address in-band RF interference where the fundamental frequency of an RF transmitter overlaps with frequencies used by a hospital wireless network or monitoring or used by other medical device wireless links.<br />\n
          The purpose of this recommended practice is to provide an ad hoc test method to estimate the electromagnetic immunity of medical devices and help identify interference issues that might exist with critical medical devices as a result of emissions from RF transmitters increasingly used in health-care facilities, particularly by doctors, staff, patients, and visitors. RF transmitters include two-way radios, walkie-talkies, mobile phones, wireless-enabled laptop computers and similar devices,1 RFID readers, networked mp3 players, two-way pagers, wireless PDAs, and wireless medical devices. The test protocol is designed to be performed as follows:<br />\n
          a) By clinical engineers, biomedical engineers, and other technical personnel<br />\n
          b) In a way that is relatively rapid and practical<br />\n
          c) In an area and with equipment that are commonly available<br />\n
          d) To identify specific effects and thresholds (i.e., transmit power and distance) to provide the basic information needed to develop a mitigation action plan<br />\n
          e) To generate test results that can be used in the formulation of policies and procedures for managing the use of RF transmitters within a health-care facility<br />\n
          A preferred method (5.6.2) and several alternative RF sources and methods (Annex C) for ad hoc testing are outlined in this recommended practice to allow flexibility with regard to the time, personnel, and resources available to perform the testing. As a result, these different options provide different levels of accuracy and comprehensiveness. The most appropriate ad hoc test strategy will depend on the needs and resources of the user of this recommended practice. This recommended practice also provides guidance for selection of the medical devices to be tested, operation of RF transmitters used as RF test sources, and assessment of test results.<br />\n
          The preferred method for evaluation in most circumstances involves the use of the actual RF transmitter(s) (e.g., mobile phones and portable and mobile radios) as test sources to generate the same RF signals that would be encountered in the health-care facility. This approach also assumes that the end user has limited time and resources, a small number of critical medical devices to test, a limited space in which to perform the testing, and a single or a small number of specific RF transmitter signals to examine. In this preferred method, the RF transmitter is placed in a constantly transmitting state (i.e., test mode). The tests can be performed with or without an electric-field-strength (E-field) meter, although the use of an E-field meter is recommended.<br />\n
          Anotherre important function of this recommended practice is to define a consistent test protocol to allow results to be obtained and compared within and across institutions. Clinical and biomedical engineers have performed their own rudimentary (“ad hoc”) electromagnetic compatibility (EMC) testing using in-house methodology, RF transmitter sources, and medical devices. As a result, a comparison of the findings between health-care organizations might not be appropriate. To facilitate a comparison between health-care organizations, it is important that the recommendations herein are followed, deviations are kept to a minimum, and the testing is performed as consistently as possible.<br />\n
          Policies and procedures for mitigation of electromagnetic interference (EMI)^2 in health-care facilities, including the use or restriction of specific RF transmitters within specific areas, often called an exclusion zone, should be based on objective information, including that obtained by the use of this test method. A common problem with exclusion zones is that they are difficult to enforce, particularly with the increasingly common use of wireless devices and their expanding variety of applications, including use in medical equipment. With regard to purchase evaluation, confirming that medical devices conform to voluntary EMC immunity standards can provide some information, although many RF transmitters are able to exceed these immunity levels greatly when held close to a medical device. This recommended practice can be used to supplement the information obtained by testing for conformance to voluntary EMC standards. A list of EMC standards and guidelines that contain radiated RF immunity requirements applicable to medical devices as well as additional background information and further recommendations for mitigation of EMI in health-care facilities are presented in the annexes.
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          This recommended practice is a guide to evaluating the electromagnetic immunity of medical devices to radiated radio-frequency (RF) emissions from common RF transmitters (e.g., two-way radios; walkie-talkies; mobile phones; wireless-enabled tablets, e-readers, laptop computers, and similar devices; radio-frequency identification (RFID) readers; networked mp3 players; two-way pagers; and wireless personal digital assistants [PDAs]). This protocol does not provide a comprehensive test or offer any guarantee, but it is a basic evaluation that can help identify medical devices that might be particularly vulnerable to interference from common RF transmitters. The ad hoc test protocol can be used to evaluate existing or newly purchased medical devices or can be implemented for the purpose of prepurchase evaluation. This recommended practice applies to medical devices used in health-care facilities, but it can also be adapted to medical devices in home health-care or mobile health-care settings. It does not apply to implantable medical devices (e.g., pacemakers and defibrillators), transport environments such as ambulances and helicopters, or RF transmitters rated at more than 8 W of output power. Testing with transmitters greater than 8 W in health-care facilities is not recommended because of possible adverse effects on critical-care medical devices that are in use in nearby areas of the facility. Finally, this recommended practice does not address in-band RF interference where the fundamental frequency of an RF transmitter overlaps with frequencies used by a hospital wireless network or monitoring or used by other medical device wireless links.<br />\n
          The purpose of this recommended practice is to provide an ad hoc test method to estimate the electromagnetic immunity of medical devices and help identify interference issues that might exist with critical medical devices as a result of emissions from RF transmitters increasingly used in health-care facilities, particularly by doctors, staff, patients, and visitors. RF transmitters include two-way radios, walkie-talkies, mobile phones, wireless-enabled laptop computers and similar devices,1 RFID readers, networked mp3 players, two-way pagers, wireless PDAs, and wireless medical devices. The test protocol is designed to be performed as follows:<br />\n
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          The purpose of this recommended practice is to provide an ad hoc test method to estimate the electromagnetic immunity of medical devices and help identify interference issues that might exist with critical medical devices as a result of emissions from RF transmitters increasingly used in health-care facilities, particularly by doctors, staff, patients, and visitors. RF transmitters include two-way radios, walkie-talkies, mobile phones, wireless-enabled laptop computers and similar devices,1 RFID readers, networked mp3 players, two-way pagers, wireless PDAs, and wireless medical devices. The test protocol is designed to be performed as follows:<br />\n
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