ISO 18113 PDF

ISO. First edition. In vitro diagnostic medical devices —. Information supplied by the manufacturer. (labelling) —. Part 1: Terms, definitions . Purchase your copy of BS EN ISO as a PDF download or hard copy directly from the official BSI Shop. All BSI British Standards. Overview. This part of ISO defines concepts, establishes general principles and specifies essential requirements for information supplied by the.

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EVS-EN ISO – Estonian Centre for Standardisation

In vitro diagnostic medical devices. 18131 website is best viewed with browser version of up to Microsoft Internet Explorer 8 or Firefox 3. Information supplied by the manufacturer labelling In vitro diagnostic reagents for professional use BS EN In vitro diagnostic instruments for professional use. Information supplied by the manufacturer labelling.

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EVS-EN ISO 18113-1:2011

Accept and continue Learn more about the cookies we use and how to change your settings. Learn more about the cookies we use and how to change your settings. Find Similar Items This product falls into the following categories. Bereitstellung von Informationen durch den Hersteller. Take the smart route to manage medical device compliance. Diagnosis medicalMedical equipment, Product information, Instructions for use, Labels, Labelling processClinical investigation instruments, Diagnostic reagents, Clinical laboratory equipment, Reagent solutions, Definitions, Measurement.

Diagnosis medicalMedical equipment, Product information, Instructions for use, Labels, Labelling processClinical investigation instruments, Clinical laboratory equipment, Health service personnel. Terms, definitions and general requirements Status: You may experience issues viewing this site in Internet Explorer 9, 10 or You may experience issues viewing this site in Internet Explorer 9, 10 or Take the smart route to manage medical device compliance.

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Information supplied by the manufacturer labelling In vitro diagnostic instruments for professional use BS EN Application of risk management to medical devices. In vitro diagnostic medical devices.

Information supplied by the manufacturer labelling. Learn more about the cookies we use and how to change your settings. Application of risk management to medical devices. You may find similar items within these categories by selecting from the choices below:.

BS EN ISO 18113-1:2011

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