BS-EN-ISO-18113-5 In vitro diagnostic medical Devices. Information supplied by the manufacturer (labelling)

BS-EN-ISO-18113-5 - 2011 EDITION - CURRENT
Show Complete Document History

Document Center Inc. is an authorized dealer of BSI standards.
The following bibliographic material is provided to assist you with your purchasing decision:

Included in this current edition are the following subparts:

 2011 EDITION - Nov. 30, 2011
 2011 EDITION CORRIGENDUM 1 - Jan. 1, 2012

Keywords

Clinical investigation instruments;Instructions for use;Product information;Medical equipment;Labels;Clinical laboratory equipment;Labelling (process);Diagnosis (medical);Consumers

To find similar documents by classification:

11.100.10 (In vitro diagnostic test systems)

This document comes with our free Notification Service, good for the life of the document.

This document is available in either Paper or PDF format.

 

Customers who bought this document also bought:

SOR/98-282
Medical Devices Regulations (Canada)

IEC-60601-1
Medical electrical equipment - Part 1: General requirements for basic safety and essential performance

BS-EN-ISO-13485
Medical devices. Quality management systems. Requirements for regulatory purposes

ORDER

Price:

$169.00        


Want this as a site license?



Document Number

BS EN ISO 18113-5:2011

Revision Level

2011 EDITION

Status

Current

Publication Date

Jan. 31, 2012

Replaces

BS EN ISO 18113-5:2009

Page Count

22

ISBN

9780580773303

International Equivalent

ISO 18113-5:2009;EN ISO 18113-5:2011

Committee Number

CH/212