BS EN 30993-5:1994, ISO 10993-5:1992 - Biological evaluation of medical devices. Tests for cytotoxicity, in vitro methods
Maintenance will be taking place for BSI Shop on Saturday 6th March 2021 between 08:00 AM and 14:00 PM UK time. During this period, BSI Shop will be unavailable or may have limited functionality. Please do not make any purchases during these works. Please accept our apologies for any inconvenience caused during this essential maintenance.

BS EN 30993-5:1994, ISO 10993-5:1992

Biological evaluation of medical devices. Tests for cytotoxicity, in vitro methods

Status : Superseded, Withdrawn   Published : July 1994 Replaced By : BS EN ISO 10993-5:1999

WITHDRAWN TITLE
*To ask about withdrawn titles contact the
Customer Relations
cservices@bsigroup.com, +44 345 086 9001





Standard NumberBS EN 30993-5:1994, ISO 10993-5:1992
TitleBiological evaluation of medical devices. Tests for cytotoxicity, in vitro methods
StatusSuperseded, Withdrawn
Publication Date15 July 1994
Withdrawn Date15 September 1999
Normative References(Required to achieve compliance to this standard)No other standards are normatively referenced
Informative References(Provided for Information)No other standards are informatively referenced
Replaced ByBS EN ISO 10993-5:1999
ReplacesBS 5736-10:1988
International RelationshipsEN 30993-5:1994,ISO 10993-5:1992
Draft Superseded By91/55176 DC
DescriptorsMedical equipment, Dental materials, Dental equipment, Cytotoxicity tests, Toxicity, Biological analysis and testing, Culture techniques, Cells (biology), Bioassay, Specimen preparation, Testing conditions
ICS11.100.20
Title in FrenchEvaluation biologique des dispositifs médicaux. Essais concernant la cytotoxicité. Méthodes in vitro
Title in GermanBiologische Beurteilung von medizinprodukten. Pruefungen auf Zytotoxizitaet: in vitro Methoden
CommitteeCH/194
ISBN0 580 23389 8
PublisherBSI
FormatA4
DeliveryNo
Pages14
File Size326.3 KB
Price£112.00


WITHDRAWN TITLE
*To ask about withdrawn titles contact the
Customer Relations
cservices@bsigroup.com, +44 345 086 9001
 Your basket
Your basket is empty

Multi-user access to over 3,500 medical device standards, regulations, expert commentaries and other documents


BSOL

Access, view and download standards with multiple user access, across multiple sites with BSOL


Develop a PAS

Develop a fast-track standardization document in 9-12 months


Tracked Changes

Understand the changes made to a standard with our new Tracked Changes version