11.040.01 : Medical equipment in general

BS EN 15986:2011

BS EN 15986:2011

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Symbol for use in the labelling of medical devices. Requirements for labelling of medical devices containing phthalates

€193.00

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UNE-EN 60601-1-6:2010

UNE-EN 60601-1-6:2010

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Medical electrical equipment -- Part 1-6: General requirements for basic safety and essential performance - Collateral standard: Usability

€79.00

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NF EN ISO 10993-13, S99-501-13 (09/2010)

NF EN ISO 10993-13, S99-501-13 (09/2010)

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Biological evaluation of medical devices - Part 13 : identification and quantification of degradation products from polymeric medical devices

€82.00

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NF EN ISO 10993-5, S99-501-5 (07/2010)

NF EN ISO 10993-5, S99-501-5 (07/2010)

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Biological evaluation of medical devices - Part 5 : tests for in vitro cytotoxicity

€107.33

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NF EN 60601-1-6, C74-016 (07/2010)

NF EN 60601-1-6, C74-016 (07/2010)

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Medical electrical equipment - Part 1-6 : general requirements for basic safety and essential performance - Collateral standard : usability

€93.67

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BS ISO 15223-2:2010

BS ISO 15223-2:2010

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Medical devices. Symbols to be used with medical device labels, labelling, and information supplied Symbol development, selection validation

€269.00

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UNE-EN 60601-1:2008 CORR:2010

UNE-EN 60601-1:2008 CORR:2010

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Medical electrical equipment -- Part 1: General requirements for basic safety and essential performance

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UNE-EN 60601-1-8:2008 CORR:2010

UNE-EN 60601-1-8:2008 CORR:2010

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Medical electrical equipment -- Part 1-8: General requirements for basic safety and essential performance - Collateral Standard: General requirements, tests and guidance for alarm systems in medical electrical equipment and medical electrical systems

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NF ISO 15223-2, S99-014-2 (03/2010)

NF ISO 15223-2, S99-014-2 (03/2010)

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Medical devices - Symbols to be used with medical device labels, labelling and information to be supplied - Part 2 : symbol development, selection and validation - Dispositifs médicaux

€82.00

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UNE-EN ISO 10993-7:2009/AC:2010

UNE-EN ISO 10993-7:2009/AC:2010

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Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals - Technical Corrigendum 1 (ISO 10993-7:2008/Cor 1:2009)

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IEC 60601-1-6:2010

IEC 60601-1-6:2010

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Medical electrical equipment - Part 1-6: General requirements for basic safety and essential performance - Collateral standard: Usability

€231.00

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ISO 15223-2:2010

ISO 15223-2:2010

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Medical devices — Symbols to be used with medical device labels, labelling, and information to be supplied Part 2: Symbol development, selection and validation

€115.00

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PD IEC/TR 80002-1:2009

PD IEC/TR 80002-1:2009

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Medical device software Guidance on the application of ISO 14971 to medical

€374.00

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IEC TR 80002-1:2009

IEC TR 80002-1:2009

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IEC TR 80002-1:2009 Medical device software - Part 1: Guidance on the application of ISO 14971 to medical device software

€418.00

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AC S99-104 (09/2009)

AC S99-104 (09/2009)

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Health products industries - Guidelines for good manufacturing practices - Synthesis and harmonization of regulatory and normative texts - Industries des produits de la santé

€200.67

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