Customer Service:
Mon - Fri: 8:30 am - 6 pm EST
Back
Standards PDF Cover Page preview

 Most recent

BS EN ISO 18113-3:2011

In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling). In vitro diagnostic instruments for professional use (British Standard)

ISO 18113-3:2009 specifies requirements for information supplied by the manufacturer of in vitro dignostic (IVD) instruments for professional use.

ISO 18113-3:2009 also applies to apparatus and equipment intended to be used with IVD instruments for professional use.

ISO 18113-3:2009 can also be applied to accessories, where appropriate.

Available for Subscriptions Available in Packages

Content Provider
British Standards Institution [bsi]

Others Also Bought

BS EN ISO 18113-1:2011
In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling). Terms, definitions and ...
Add to cart
BS EN ISO 18113-2:2011
In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling). In vitro diagnostic ...
Add to cart
BS EN ISO 18113-4:2011
In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling). In vitro diagnostic ...
Add to cart
Document History
Revises:
Included in Packages
This standard is also available in these packages:
Amendments & Corrections
We have no amendments or corrections for this standard.
ANSI Logo

As the voice of the U.S. standards and conformity assessment system, the American National Standards Institute (ANSI) empowers its members and constituents to strengthen the U.S. marketplace position in the global economy while helping to assure the safety and health of consumers and the protection of the environment.

Useful Links
CUSTOMER SERVICE
NEW YORK OFFICE
ANSI HEADQUARTERS
2024 © American National Standards Institute (ANSI) All Rights Reserved.