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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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. Information supplied 188113 the manufacturer labelling.

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EVS-EN ISO – Estonian Centre for Standardisation

Terms, definitions and general requirements. We use cookies to make our website easier to use and to better understand your needs. In vitro diagnostic medical devices. Application of risk management to medical devices. Find Similar Items This product falls into the following categories. You may find similar items within these categories by selecting from the choices below:.

In vitro diagnostic instruments for professional use Status: Diagnosis medicalMedical equipment, Product information, Instructions for use, Labels, Labelling processClinical investigation instruments, Diagnostic reagents, Clinical laboratory equipment, Reagent solutions, Definitions, Measurement.

Find Similar Items This product falls into the following categories. Learn more about the cookies we use and how to change your settings.

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EVS-EN ISO 18113-1:2011

Take the smart route to manage medical device compliance. In vitro diagnostic medical devices. Bereitstellung von Informationen durch den Hersteller. Search all products by. This website is best viewed with browser version of up to Microsoft Internet Explorer 8 or Firefox 3.

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Application of risk management to medical devices. Begriffe und allgemeine Anforderungen. Your basket is empty.

BS EN ISO – In Vitro Diagnostic Medical Devices Package

Bereitstellung von Informationen durch den Hersteller. Terms, definitions and general requirements Status: Information supplied by the manufacturer labelling In vitro diagnostic instruments for professional use BS EN Learn more about the cookies we use and how to change your settings. The faster, easier way to work with standards. Click to learn more. Information supplied by the manufacturer labelling. Please download Chrome or Firefox or view our browser tips.

The faster, easier way to work with standards. 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 Take the smart route to manage medical device compliance.