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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Find Similar Items This product falls into the following categories. Accept and continue Learn more about the cookies we use and how to change your settings. Diagnosis medicalMedical equipment, Product information, Instructions for use, Labels, Labelling processClinical investigation instruments, Clinical laboratory equipment, Health service personnel.

This website is best viewed with browser version of up to Microsoft Internet Explorer 8 or Firefox 3. Diagnosis medicalMedical equipment, Product information, Instructions for use, Labels, Labelling processClinical investigation instruments, Diagnostic reagents, Clinical laboratory equipment, Reagent solutions, Definitions, Measurement.

BS EN ISO – In Vitro Diagnostic Medical Devices Package

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Terms, definitions and general requirements Status: Find Similar Items This product falls into the following categories. We use cookies to make our website easier to use and to better understand your needs.

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BS EN ISO 18113-3:2011

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BS EN ISO 18113-1:2011

Learn more about the cookies we use and how to change your settings. Take the smart route to manage medical device compliance. This website is best viewed with browser version of up to Microsoft Internet Explorer 8 or Firefox 3. The faster, easier way to work with standards. You may find similar items within these categories by selecting from the choices below:. Bereitstellung von Informationen durch den Hersteller. In vitro diagnostic instruments for professional use Status: In vitro diagnostic instruments for professional use.

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Begriffe und allgemeine Anforderungen. Information supplied by the manufacturer labelling. You may experience issues viewing this site in Internet Explorer 9, 10 or We use cookies to make our website easier to use and to better understand your needs. Information supplied by the manufacturer labelling In vitro diagnostic reagents for professional use BS EN Application isi risk management to medical devices.

In vitro diagnostic medical devices. Information supplied by the manufacturer labelling.

Please download Chrome or Firefox or view our browser tips. Take the smart route to manage medical device compliance. Click to learn more. Bereitstellung von Informationen durch den Hersteller. Information supplied by the manufacturer labelling In vitro diagnostic instruments for professional use BS EN You may find similar items within these 118113 by selecting from the choices below:.

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