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

Your basket is empty. Please download Chrome or Firefox or view our browser tips. Application of risk management to medical devices. The faster, easier way to work with standards. Information supplied by the manufacturer labelling.

Begriffe und allgemeine Anforderungen. You may find similar items within these categories by selecting from the choices below:. In vitro diagnostic instruments for professional use.

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Accept and continue Learn more about the cookies we use and how to change your settings. Information supplied by the manufacturer labelling. Click to learn more. Diagnosis medicalMedical equipment, Product information, Instructions for use, Labels, Labelling processClinical investigation instruments, Diagnostic reagents, Clinical laboratory equipment, Reagent solutions, Definitions, Measurement.

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EVS-EN ISO 18113-1:2011

Application of risk management to medical devices. Search all products by. Take the smart route to manage medical device compliance. Click to learn more. You may experience issues viewing this site in Internet Explorer 9, 10 or Information supplied by the manufacturer labelling In vitro diagnostic reagents for professional use BS EN In vitro diagnostic instruments ixo professional use Status: This website is best viewed with browser version of up to Microsoft Internet Explorer 8 or Firefox 3.

Terms, definitions and general requirements Status: Bereitstellung von Informationen durch den Hersteller. Information supplied by the manufacturer labelling In vitro diagnostic instruments for professional use BS EN We use cookies to make our website easier to 18113 and to better understand your needs.

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You may find similar items within these categories by selecting from the isp below:. Take the smart route to manage medical device compliance. In vitro diagnostic medical devices. Bereitstellung von Informationen durch den Hersteller. Terms, definitions and general requirements. Learn more about the cookies we use and how to change your settings. The faster, easier way to work with standards.

Is medicalMedical equipment, Product information, Instructions for use, Labels, Labelling processClinical investigation instruments, Clinical laboratory equipment, Health service personnel. Find Similar Items This product falls into the following categories. Find Similar Items This product falls into the following categories. This website is best viewed with browser version of up to Microsoft Internet Explorer 8 or Firefox 3.