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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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Begriffe und allgemeine Anforderungen. Application of risk management to medical devices. 1811 and continue Learn more about the cookies we use and how to change your settings.

This website is best viewed kso browser version of up to Microsoft Internet Explorer 8 or Firefox 3. Learn more about the cookies we use and how to change your settings. Please download Chrome or Firefox or view our browser tips. You may experience issues viewing this site in Internet Explorer 9, 10 or In vitro diagnostic medical devices. Take the smart route to manage medical device compliance.

BS EN ISO 18113-1:2011

In vitro diagnostic medical devices. Click to learn more.

Accept and continue Learn more about the cookies we use and how to change your settings. Io use cookies to make our website easier to use and to better understand your needs. Find Similar Items This product falls into the following categories. Application of risk management to ieo devices. 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 This website is best viewed with browser version of up to Microsoft Internet Explorer 8 or Firefox 3. Information supplied by the manufacturer labelling In vitro diagnostic instruments for professional use BS EN 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:. Terms, definitions and general requirements Status: Click to learn more.

BS EN ISO – In Vitro Diagnostic Medical Devices Package

You may experience issues viewing this site in Internet Explorer kso, 10 or Take the smart route to manage medical device compliance. Diagnosis medicalMedical equipment, Product information, Instructions for use, Labels, Labelling processClinical investigation instruments, Diagnostic reagents, Clinical laboratory equipment, Reagent solutions, Definitions, Measurement.

Bereitstellung von Informationen durch den Hersteller. Terms, definitions and general requirements. The faster, easier way to work with standards.