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 18113-1:2011

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EVS-EN ISO – Estonian Centre for Standardisation

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Terms, definitions and general requirements. 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. Accept and continue Learn more about the cookies we use and how to change your settings. In vitro diagnostic instruments for professional use. Search all products by. 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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Terms, definitions and general requirements Status: The faster, easier way to work with standards. In vitro diagnostic medical devices. Begriffe und allgemeine Anforderungen. Bereitstellung von Informationen durch den Hersteller.

Please download Chrome or Firefox or view our browser tips. This website is best viewed with browser version of up to Microsoft Internet Explorer 8 or Firefox 3. Information supplied by the manufacturer labelling. Click to learn more. Application of risk management to medical devices.

BS EN ISO – In Vitro Diagnostic Medical Devices Package

ios Diagnosis medicalMedical equipment, Product information, Instructions for use, Labels, Labelling processClinical investigation instruments, Clinical laboratory equipment, Health service personnel.

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