BS EN ISO 10993-1:2003 - Biological evaluation of medical devices. Evaluation and testing

BS EN ISO 10993-1:2003

Biological evaluation of medical devices. Evaluation and testing

Status : Superseded, Withdrawn   Published : October 2003 Replaced By : BS EN ISO 10993-1:June 2009, BS EN ISO 10993-1:October 2009

WITHDRAWN TITLE
*To ask about withdrawn titles contact the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





Standard NumberBS EN ISO 10993-1:2003
TitleBiological evaluation of medical devices. Evaluation and testing
StatusSuperseded, Withdrawn
Publication Date09 October 2003
Withdrawn Date31 July 2009
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 10993-1:June 2009, BS EN ISO 10993-1:October 2009
ReplacesBS EN ISO 10993-1:1998
International RelationshipsEN ISO 10993-1:2003,ISO 10993-1:2003
DescriptorsDental equipment, Biological analysis and testing, Biological hazards, Bioassay, Clinical investigation instruments, Dental materials, Cytotoxicity tests, Medical technology, Contaminants, Medical instruments, Compatibility, Implants (surgical), Medical equipment
ICS11.100.20
Title in FrenchEvaluation biologique des dispositifs medicaux. Evaluation et essais
Title in GermanBiologische Beurteilung von Medizinprodukten. Beurteilung und Pruefungen
CommitteeCH/194
ISBN0 580 42731 5
PublisherBSI
FormatA4
DeliveryNo
Pages26
File Size771 KB
Price£182.00


WITHDRAWN TITLE
*To ask about withdrawn titles contact the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


Worldwide Standards
We can source any standard from anywhere in the world


Tracked Changes

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


BSOL

The faster, easier way to work with standards


Customers who bought this product also bought

  • BS EN 556-1:2001
    Sterilization of medical devices. Requirements for medical devices to be designated "STERILE" Requirements for terminally sterilized medical devices
  • BS EN ISO 17665-1:2006
    Sterilization of health care products. Moist heat Requirements for the development, validation and routine control of a sterilization process for medical devices
  • BS EN 13975:2003
    Sampling procedures used for acceptance testing of in vitro diagnostic medical devices. Statistical aspects