Please select and order
€72.72
excl. VAT
CONFIGURE NOW
Norm
ÖNORM EN ISO 22794
Issue date: 2010 01 15
Dentistry - Implantable materials for bone filling and augmentation in oral and maxillofacial surgery - Contents of a technical file (ISO 22794:2007, corrected version 2009-01-15)
This International Standard applies to implantable materials, whether resorbable or non-resorbable, used as dental devices for filling and augmenting bones in oral and ma...
Read more
Valid
Publisher:
Austrian Standards International
Format:
Digital | 14 Pages
Language:
German
| English
| Download GER/ENG
Optionally co-design standards:
ICS
This International Standard applies to implantable materials, whether resorbable or non-resorbable, used as dental devices for filling and augmenting bones in oral and maxillofacial surgery. Products that are essentially pure (> 90 %) hydroxyapatite are not covered by this International Standard. Evaluation includes the physico-chemical, mechanical, biological and clinical aspects and behaviour of these implantable dental materials. Materials such as autografts, allografts and membranes, and products for which the primary intended use is to deliver a medicinal product, are not covered by this International Standard.
ÖNORM EN ISO 22794
2010 01 15
Dentistry - Implantable materials for bone filling and augmentation in oral and maxillofacial surger...
Norm
↖
ÖNORM EN ISO 22794
2007 10 01
Dentistry - Implantable materials for bone filling and augmentation in oral and maxillofacial surger...
Norm
Norm
ISO 10993-1:2009
Issue date :
2009 10 13
Biological evaluation of medical devices — Part 1: Evaluation and testing within a risk management process
Norm
ISO 10993-17:2002
Issue date :
2002 11 27
Biological evaluation of medical devices — Part 17: Establishment of allowable limits for leachable substances
Norm
ISO 11135-1:2007
Issue date :
2007 04 27
Sterilization of health care products — Ethylene oxide — Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices (Corrected version 2007-10)
Norm
ISO 11137-1:2006
Issue date :
2006 04 19
Sterilization of health care products — Radiation — Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices
Norm
ISO 11607-2:2006
Issue date :
2006 04 07
Packaging for terminally sterilized medical devices — Part 2: Validation requirements for forming, sealing and assembly processes
Norm
ISO 13408-1:2008
Issue date :
2008 06 10
Aseptic processing of health care products — Part 1: General requirements
Norm
ISO 14155-1:2003
Issue date :
2003 02 26
Clinical investigation of medical devices for human subjects — Part 1: General requirements
Norm
ISO 14155-2:2003
Issue date :
2003 05 16
Clinical investigation of medical devices for human subjects — Part 2: Clinical investigation plans
Norm
ISO 14937:2009
Issue date :
2009 10 14
Sterilization of health care products — General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices
Norm
ISO 14971:2007
Issue date :
2007 02 28
Medical devices — Application of risk management to medical devices (Corrected version 2007-09)
Norm
ISO 17665-1:2006
Issue date :
2006 08 17
Sterilization of health care products — Moist heat — Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices
Norm
ÖNORM EN 1041
Issue date :
2008 11 01
Information supplied by the manufacturer with medical devices
Norm
ISO 10993-17:2002
Issue date :
2002 11 27
Biological evaluation of medical devices — Part 17: Establishment of allowable limits for leachable substances
Norm
ISO 11135-1:2007
Issue date :
2007 04 27
Sterilization of health care products — Ethylene oxide — Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices (Corrected version 2007-10)
Norm
ISO 11137-1:2006
Issue date :
2006 04 19
Sterilization of health care products — Radiation — Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices
Norm
ISO 11607-2:2019
Issue date :
2019 01 31
Packaging for terminally sterilized medical devices — Part 2: Validation requirements for forming, sealing and assembly processes
Norm
ISO 13408-1:2008
Issue date :
2008 06 10
Aseptic processing of health care products — Part 1: General requirements
Norm
ISO 14155-1:2003
Issue date :
2003 02 26
Clinical investigation of medical devices for human subjects — Part 1: General requirements
Norm
ISO 14155-2:2003
Issue date :
2003 05 16
Clinical investigation of medical devices for human subjects — Part 2: Clinical investigation plans
Norm
ISO 14937:2009
Issue date :
2009 10 14
Sterilization of health care products — General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices
Norm
ISO 14971:2019
Issue date :
2019 12 10
Medical devices — Application of risk management to medical devices
Norm
ISO 15223:2000
Issue date :
2000 04 13
Medical devices — Symbols to be used with medical device labels, labelling and information to be supplied
Norm
ISO 17665-1:2006
Issue date :
2006 08 17
Sterilization of health care products — Moist heat — Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices