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 18113-1:2011

Application of risk management to medical devices. Begriffe und allgemeine Anforderungen. Bereitstellung von Informationen durch den Hersteller. Your basket is empty. Application of risk management to medical devices. Search all products by. Information supplied by the manufacturer labelling In vitro diagnostic instruments for professional use BS EN Search all products by.

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BS EN ISO – In Vitro Diagnostic Medical Devices Package

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Information supplied by the manufacturer labelling. Diagnosis medicalMedical equipment, Product information, Instructions for use, Labels, Labelling processClinical investigation instruments, Diagnostic reagents, Clinical laboratory equipment, Reagent solutions, Definitions, Measurement. You may find similar items within these categories by selecting from the choices below:.

You may find similar items within these categories by selecting from the choices below:. The faster, easier way to work with standards. Accept and continue Learn more about the cookies we use and how to change your settings. We use cookies to make our website easier to use and to better understand your needs. In vitro diagnostic medical devices.