June 18, 2020

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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BS EN ISO – In Vitro Diagnostic Medical Devices Package

Search all products by. Find Similar Items This product falls into the following categories. You may find similar items within these categories by selecting from the choices below:. Information supplied by the manufacturer labelling.

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Terms, definitions and general requirements Status: Click to learn more. Bereitstellung von Informationen durch den Hersteller. Your basket is empty. Take the smart route to manage medical device compliance. The faster, easier way to work with standards. Information supplied by the manufacturer labelling In vitro diagnostic isp for professional use BS EN Application of risk management to medical devices.

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EVS-EN ISO – Estonian Centre for Standardisation

Accept and continue Learn more about the cookies we use and how to change your settings. In vitro diagnostic medical devices. Terms, definitions and general requirements.

Diagnosis medicalMedical equipment, Product information, Instructions for use, Labels, Labelling processClinical investigation instruments, Diagnostic reagents, Clinical laboratory equipment, Reagent solutions, Definitions, Measurement. Begriffe und allgemeine Anforderungen.

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