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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In vitro diagnostic medical devices.

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EVS-EN ISO 18113-1:2011

Diagnosis medicalMedical equipment, Product information, Jso for use, Labels, Labelling processClinical investigation instruments, Diagnostic reagents, Clinical laboratory equipment, Reagent solutions, Definitions, Measurement. 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 instruments for professional use BS EN The faster, easier way to work with standards.

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BS EN ISO 18113-1:2011

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EVS-EN ISO – Estonian Centre for Standardisation

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

Information supplied by the manufacturer labelling In vitro diagnostic reagents for professional use BS EN In vitro diagnostic instruments for professional use Status: You may find similar items within these categories by selecting from the choices below:.

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BS EN ISO – In Vitro Diagnostic Medical Devices Package

The faster, easier way to work with standards. Bereitstellung von Informationen durch den Hersteller. This website is best viewed with 11813 version of up to Microsoft Internet Explorer 8 or Firefox 3.

Search all products by. In vitro diagnostic instruments for professional use. You may experience issues viewing this site in Internet Explorer 9, 10 or Find Similar Items This product falls into the following categories. Terms, definitions and general requirements.

Bereitstellung von Informationen durch 81113 Hersteller. Accept and continue Learn more about the cookies we use and how to change your settings. Application of risk management to medical devices. Terms, definitions and general requirements Status: