BS EN 550:1994 - Sterilization of medical devices. Validation and routine control of ethylene oxide sterilization

BS EN 550:1994

Sterilization of medical devices. Validation and routine control of ethylene oxide sterilization

Status : Superseded, Withdrawn   Published : October 1994 Replaced By : BS EN ISO 11135-1:2007

WITHDRAWN TITLE
*To ask about withdrawn titles contact the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


Provides requirements and guidance




Standard NumberBS EN 550:1994
TitleSterilization of medical devices. Validation and routine control of ethylene oxide sterilization
StatusSuperseded, Withdrawn
Publication Date15 October 1994
Confirm Date01 March 2005
Withdrawn Date04 May 2010
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 11135-1:2007
International RelationshipsEN 550:1994
Draft Superseded By91/57776 DC
DescriptorsMedical equipment, Sterilization (hygiene), Ethylene oxide, Hygiene, Medical instruments, Sterile equipment, Performance, Performance testing, Quality control, Maintenance, Acceptance (approval), Specimen preparation, Test equipment
ICS11.080.01
Title in FrenchSterilisation de dispositifs medicaux. Validation et controle de routine pour la sterilisation a l'oxyde d'ethylene
Title in GermanSterilisation von Medizinprodukten. Validierung nd Routineueberwachung fuer die Sterilisation mit Ethylenoxid / Referenz: 90/385/EWG, 93/42/EWG
CommitteeCH/198
ISBN0 580 23201 8
PublisherBSI
FormatA4
DeliveryNo
Pages30
File Size496.7 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WITHDRAWN TITLE
*To ask about withdrawn titles contact the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


BSOL

The faster, easier way to work with standards


Develop a PAS

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


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


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 ISO 11135-1:2007
    Sterilization of health care products. Ethylene oxide Requirements for development, validation and routine control of a sterilization process for medical devices