BS-EN-ISO-18113-3 › In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling)
Document Center Inc. is an authorized dealer of BSI standards.
The following bibliographic material is provided to assist you with your purchasing decision:
The following bibliographic material is provided to assist you with your purchasing decision:
In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling)
Keywords
Health service personnel;Instructions for use;Clinical laboratory equipment;Medical equipment;Product information;Labelling (process);Labels;Clinical investigation instruments;Diagnosis (medical)
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:
BS-EN-ISO-14971Medical devices. Application of risk management to medical devices
BS-EN-ISO-13485
Medical devices. Quality management systems. Requirements for regulatory purposes
SOR/98-282
Medical Devices Regulations (Canada)
Document Number
BS EN ISO 18113-3:2024
Revision Level
2024 EDITION
Status
Current
Publication Date
June 12, 2024
Replaces
BS EN ISO 18113-3:2011
Page Count
26
ISBN
9780539134803
International Equivalent
EN ISO 18113-3;ISO 18113-3
Committee Number
CH/212