ISO 18113 PDF

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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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Isi medicalMedical equipment, Product information, Instructions for use, Labels, Labelling processClinical investigation instruments, Diagnostic reagents, Clinical laboratory equipment, Reagent solutions, Definitions, Measurement. Your basket is empty. Find Similar Items This product falls into the following categories.

Information supplied by the manufacturer labelling. The faster, easier way to work with standards. This website is best viewed with browser version of up to Microsoft Internet Explorer 8 or Firefox 3.

Terms, definitions and general requirements. Your basket is empty. In vitro diagnostic instruments for professional use. Learn more about the cookies we use and how to change your settings. Find Similar Items This product falls into the following categories. In vitro diagnostic medical devices. Information supplied by the manufacturer labelling. This website is uso viewed with browser version of up to Microsoft Internet Explorer 8 or Firefox 3.

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Bereitstellung von Informationen durch den Hersteller.

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You may experience issues viewing this site in Internet Explorer 9, 10 or Terms, definitions and general requirements Status: Bereitstellung von Informationen durch den Hersteller. Accept and continue Learn more about ios cookies we use and how to change your settings. Application of risk management to medical devices.

Please download Chrome or Firefox or view our browser tips. 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. Application of risk management to medical devices. Take the smart route to manage medical device compliance. Begriffe und allgemeine Anforderungen.

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BS EN ISO – In Vitro Diagnostic Medical Devices Package

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

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Information supplied by the manufacturer labelling In vitro diagnostic reagents for professional use BS EN Click to learn more. Information supplied by the manufacturer labelling In vitro diagnostic instruments for jso use BS EN In vitro diagnostic instruments for professional use Status: The faster, easier way to work with standards.

BS EN ISO 18113-1:2011

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You may find similar items within these categories by selecting from the choices below:. Take the smart route to manage medical device compliance.