BS EN ISO 14971:2007 - Medical devices. Application of risk management to medical devices

BS EN ISO 14971:2007

Medical devices. Application of risk management to medical devices

Status : Revised, Superseded, Withdrawn   Published : April 2007 Replaced By : BS EN ISO 14971:2009

WITHDRAWN TITLE
*To ask about withdrawn titles contact the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





Standard NumberBS EN ISO 14971:2007
TitleMedical devices. Application of risk management to medical devices
StatusRevised, Superseded, Withdrawn
Publication Date30 April 2007
Withdrawn Date31 July 2009
Normative References(Required to achieve compliance to this standard)No other standards are normatively referenced
Informative References(Provided for Information)90/285/EEC, ISO 10993-2, IEC 61882, ISO 17593, 93/42/EEC, ISO 18153, ISO 19001, IEC 62366, ISO 22442, ISO 9000:2005, ISO 13485:2003, ISO 15197, IEC 60601-1:2005, ISO 18113-1, ISO 15189, EN 12442-1, ISO 10993-1, ISO 14155-2, IEC 60601-1-6, IEC 61025, ISO 10993-17, IEC 60601-1-8, ISO 9001:1994, IEC 60812, IEC 60300-3-9:1995, IEC/TR 60513, ISO 9000-3:1997, EN 1441:1997, ISO 17511, ISO/TR 14969, 93/68/EEC, ISO 15198, ISO/IEC Guide 51:1999, 98/79/EC, IEC 60601-1-4, ISO 14155-1, ISO/IEC Guide 2:1996, IEC 60050-191, 90/385/EEC
Replaced ByBS EN ISO 14971:2009
International RelationshipsEN ISO 14971:2007,ISO 14971:2007
Draft Superseded By05/30140005 DC
DescriptorsMedical instruments, Management, Safety measures, Risk assessment, Medical equipment, Clinical investigation instruments, Diagnosis (medical), Risk analysis, Hazards
ICS11.040.01
Title in FrenchDispositifs médicaux. Application de la gestion des risques aux dispositifs médicaux
Title in GermanMedizinprodukte. Anwendung des Risikomanagements auf Medizinprodukte
CommitteeCH/210/4
ISBN978 0 580 50605 5
PublisherBSI
FormatA4
DeliveryNo
Pages94
File Size1.737 MB
Price£274.00


WITHDRAWN TITLE
*To ask about withdrawn titles contact the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


Develop a PAS

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


BSOL

The faster, easier way to work with standards


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 14644-5:2004
    Cleanrooms and associated controlled environments Operations
  • BS EN 13612:2002
    Performance evaluation of in vitro diagnostic medical devices