11.060.15 牙科植入物 标准查询与下载
共找到 145 条与 牙科植入物 相关的标准，共 10 页
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)
- ICS
- 11.060.15
- CCS
- 发布
- 2009-12-15
- 实施
- 2009-12-15
Dentistry - Implantable materials for bone filling and augmentation in oral and maxillofacial surgery - Contents of a technical file.
- ICS
- 11.060.15
- CCS
- C33
- 发布
- 2009-12-01
- 实施
- 2009-12-25
This European Standard specifies general requirements for dental implants and accessories. Surgically implantable dental materials defined as restorative materials are specifically excluded and described in EN 1641. This European Standard includes requirements for intended performance, design attributes, components, sterilization, packaging, marking, labelling, and information supplied by the manufacturer.
Dentistry - Medical devices for dentistry - Dental implants
- ICS
- 11.060.15
- CCS
- C33
- 发布
- 2009-11-30
- 实施
- 2009-11-30
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 ciinical 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.
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); English version of DIN EN ISO 22794:2009-11
- ICS
- 11.060.15
- CCS
- C33
- 发布
- 2009-11
- 实施
이 표준은 구강악안면외과에서 골 충전 및 증대용 치과의료기기로 사용되는 흡수성 또는 비흡수
Dentistry－Implantable materials for bone filling and augmentation in oral and maxillofacial surgery－Contents of a technical file
- ICS
- 11.060.15
- CCS
- C33
- 发布
- 2009-10-27
- 实施
- 2009-10-27
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.
Dentistry - Implantable materials for bone filling and augmentation in oral and maxillofacial surgery - Contents of a technical file
- ICS
- 11.060.15
- CCS
- 发布
- 2009-10-12
- 实施
- 2009-10-12
Dentistry. Implantable materials for bone filling and augmentation in oral and maxillofacial surgery. Contents of a technical file
- ICS
- 11.060.15
- CCS
- C33
- 发布
- 2009-09-30
- 实施
- 2009-09-30
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 byThis International Standard.
Dentistry - Implantable materials for bone filling and augmentation in oral and maxillofacial surgery - Contents of a technical file
- ICS
- 11.060.15
- CCS
- 发布
- 2009-08-01
- 实施
Dentistry - Test methods for posts and cores
- ICS
- 11.060.15
- CCS
- C33
- 发布
- 2009-03
- 实施
Dentistry - Implants - Dynamic fatigue test for endosseous dental implants (ISO 14801:2007)
- ICS
- 11.060.15
- CCS
- 发布
- 2008-02-28
- 实施
- 2008-02-28
This Internahonal Standard specifies a method of fatigue testing of single post endosseous dental implants of the transmucosal type and their premanufactured prosthetic components. It is most useful for comparing endosseous dental implants of different designs or sizes. While this International Standard simulates the functional loading of an endosseous dental implant body and its premanufactured prosthetic components under "worst case" conditions, it is not applicable for predicting the in vivo performance of an endosseous dental implant or prosthesis, particularly if more than one implant is used for a prosthesis.
Dentistry - Implants - Dynamic fatigue test for endosseous dental implants (ISO 14801:2007); English version of DIN EN ISO 14801:2008-02
- ICS
- 11.060.15
- CCS
- C33
- 发布
- 2008-02
- 实施
This International Standard specifies a method of fatigue testing of single post endosseous dental implants of the transmucosal type and their premanufactured prosthetic components. It is most useful for comparing endosseous dental implants of different designs or sizes.While it simulates the functional loading of an endosseous dental implant body and its premanufactured prosthetic components under “worst case” conditions, this International Standard is not applicable for predicting the in vivo performance of an endosseous dental implant or prosthesis, particularly if multiple endosseous dental implants are used for a prosthesis.
Dentistry - Implants - Dynamic fatigue test for endosseous dental implants
- ICS
- 11.060.15
- CCS
- 发布
- 2008-01-11
- 实施
- 2008-01-11
Dentistry - Implants - Dynamic fatigue test for endosseous dental implants.
- ICS
- 11.060.15
- CCS
- C33
- 发布
- 2008-01-01
- 实施
- 2008-01-12
Dentistry. Artificial teeth for dental prostheses. Technical requirements. Test methods
- ICS
- 11.060.15
- CCS
- 发布
- 2008
- 实施
- 2009-09-01
ISO 14801:2007 specifies a method of fatigue testing of single post endosseous dental implants of the transmucosal type and their premanufactured prosthetic components. It is most useful for comparing endosseous dental implants of different designs or sizes. While it simulates the functional loading of an endosseous dental implant body and its premanufactured prosthetic components under “worst case” conditions, ISO 14801:2007 is not applicable for predicting the in vivo performance of an endosseous dental implant or prosthesis, particularly if multiple endosseous dental implants are used for a prosthesis.
Dentistry - Implants - Dynamic fatigue test for endosseous dental implants
- ICS
- 11.060.15
- CCS
- C33
- 发布
- 2007-12-31
- 实施
- 2007-12-31
This International Standard specifies a method of fatigue testing of single post endosseous dental implants of the transmucosal type and their premanufactured prosthetic components. It is most useful for comparing endosseous dental implants of different designs or sizes. While this International Standard simulates the functional loading of an endosseous dental implant body and its premanufactured prosthetic components under “worst case” conditions, it is not applicable for predicting the in vivo performance of an endosseous dental implant or prosthesis, particularly if more than one implant is used for a prosthesis.
Dentistry - Implants - Dynamic fatigue test for endosseous dental implants
- ICS
- 11.060.15
- CCS
- C33
- 发布
- 2007-11
- 实施
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 .Porducts that are essentially pure(>90%)hydroxyapatite are not covered by this international Standard. Enaluation 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 internation Standard.
Dentistry - Implantable materials for bone filling and augmentation in oral and maxillofacial surgery - Contents of a technical file (ISO 22794:2007); German version EN ISO 22794:2007
- ICS
- 11.060.15
- CCS
- C33
- 发布
- 2007-10
- 实施
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.
Dentistry - Implantable materials for bone filling and augmentation in oral and maxillofacial surgery - Contents of a technical file
- ICS
- 11.060.15
- CCS
- C33
- 发布
- 2007-08-31
- 实施
- 2007-08-31
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.
Dentistry - Implantable materials for bone filling and augmentation in oral and maxillofacial surgery - Contents of a technical file
- ICS
- 11.060.15
- CCS
- C33
- 发布
- 2007-07
- 实施
