ISO 5832-7:2016
Withdrawn
A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.
View Superseded by
Implants for surgery — Metallic materials — Part 7: Forgeable and cold-formed cobalt-chromium-nickel-molybdenum-iron alloy
Hardcopy , PDF
English, French
14-11-2016
09-04-2025
ISO 5832-7:2016 specifies the characteristics of, and corresponding test methods for, forgeable and cold-formed cobalt-chromium-nickel-molybdenum-iron alloy for use in the manufacture of surgical implants.
| Committee |
ISO/TC 150/SC 1
|
| DevelopmentNote |
Supersedes ISO/DIS 5832-7. (11/2016)
|
| DocumentType |
Standard
|
| Pages |
3
|
| PublisherName |
International Organization for Standardization
|
| Status |
Withdrawn
|
| SupersededBy | |
| Supersedes |
| Standards | Relationship |
| DS/EN ISO 5832-7:2019 | Identical |
| ÖNORM EN ISO 5832-7: 2019 11 15 | Identical |
| NEN-EN-ISO 5832-7:2019 | Identical |
| BS ISO 5832-7:2016 | Identical |
| NF ISO 5832-7 : 2017 | Identical |
| NEN ISO 5832-7 : 2016 | Identical |
| EN ISO 5832-7:2019 | Identical |
| SS-EN ISO 5832-7:2019 | Identical |
| I.S. EN ISO 5832-7:2019 | Identical |
| BS EN ISO 5832-7:2019 | Identical |
| NF EN ISO 5832-7:2019 | Identical |
| DIN EN ISO 5832-7:2019-12 | Identical |
| NS-EN ISO 5832-7:2019 | Identical |
| DIN ISO 5832-7:2017-09 | Identical |
| PN-EN ISO 5832-7:2020-03 | Identical |
| DS ISO 5832-7 : 2016 | Identical |
| GOST R ISO 5832-7 : 2009 | Identical |
| UNE-EN ISO 5832-7:2020 | Identical |
| BIS IS 5347-8 : 1997(R2003) | Identical |
| DIN ISO 5832-7:2001-07 | Identical |
| 11/30242625 DC : 0 | BS ISO 5838-1 - IMPLANTS FOR SURGERY - METALLIC SKELETAL PINS AND WIRES - PART 1: GENERAL REQUIREMENTS |
| BS ISO 5838-1:2013 | Implants for surgery. Metallic skeletal pins and wires General requirements |
| BS ISO 15374:1998 | Implants for surgery. Requirements for production of forgings |
| BS ISO 12891-2:2014 | Retrieval and analysis of surgical implants Analysis of retrieved surgical implants |
| DIN EN ISO 16061:2015-09 | Instrumentation for use in association with non-active surgical implants - General requirements (ISO 16061:2015) |
| DIN EN ISO 9713:2009-08 | Neurosurgical implants - Self-closing intracranial aneurysm clips (ISO 9713:2002) |
| BS EN ISO 9713:2009 | Neurosurgical implants. Self-closing intracranial aneurysm clips |
| BS EN ISO 10993-6:2016 | Biological evaluation of medical devices Tests for local effects after implantation |
| BS EN 12010:1998 | Non-active surgical implants. Joint replacement implants. Particular requirements |
| I.S. EN ISO 10993-6:2016 | BIOLOGICAL EVALUATION OF MEDICAL DEVICES - PART 6: TESTS FOR LOCAL EFFECTS AFTER IMPLANTATION (ISO 10993-6:2016) |
| I.S. EN ISO 9713:2009 | NEUROSURGICAL IMPLANTS - SELF-CLOSING INTRACRANIAL ANEURYSM CLIPS |
| NF EN ISO 9713 : 2009 | NEUROSURGICAL IMPLANTS - SELF-CLOSING INTRACRANIAL ANEURYSM CLIPS |
| ANSI/AAMI/ISO 10993-6:2016 | BIOLOGICAL EVALUATION OF MEDICAL DEVICES - PART 6: TESTS FOR LOCAL EFFECTS AFTER IMPLANTATION |
| ISO 15374:1998 | Implants for surgery — Requirements for production of forgings |
| 99/565665 DC : DRAFT NOV 1999 | BS ISO 9713 NEUROSURGICAL IMPLANTS - SELF-CLOSING INTRACRANIAL ANEURYSM CLIPS |
| 14/30261590 DC : 0 | BS EN ISO 10993-6 - BIOLOGICAL EVALUATION OF MEDICAL DEVICES - PART 6: TESTS FOR LOCAL EFFECTS AFTER IMPLANTATION |
| 13/30242622 DC : 0 | BS ISO 12891-2 - RETRIEVAL AND ANALYSIS OF SURGICAL IMPLANTS - PART 2: ANALYSIS OF RETRIEVED SURGICAL IMPLANTS |
| ISO 12891-2:2014 | Retrieval and analysis of surgical implants — Part 2: Analysis of retrieved surgical implants |
| I.S. EN ISO 16061:2015 | INSTRUMENTATION FOR USE IN ASSOCIATION WITH NON-ACTIVE SURGICAL IMPLANTS - GENERAL REQUIREMENTS (ISO 16061:2015) |
| ISO 16061:2015 | Instrumentation for use in association with non-active surgical implants — General requirements |
| BS EN 30993-6:1995 | Biological evaluation of medical devices Tests for local effects after implantation |
| EN ISO 10993-6:2016 | Biological evaluation of medical devices - Part 6: Tests for local effects after implantation (ISO 10993-6:2016) |
| EN ISO 9713:2009 | Neurosurgical implants - Self-closing intracranial aneurysm clips (ISO 9713:2002) |
| BS EN ISO 16061:2015 | Instrumentation for use in association with non-active surgical implants. General requirements |
| ASTM F 1058 : 2016 : REDLINE | Standard Specification for Wrought 40Cobalt-20Chromium-16Iron-15Nickel-7Molybdenum Alloy Wire, Strip, and Strip Bar for Surgical Implant Applications (UNS R30003 and UNS R30008) |
| ASTM F 2527 : 2016 : REDLINE | Standard Specification for Wrought Seamless and Welded and Drawn Cobalt Alloy Small Diameter Tubing for Surgical Implants (UNS R30003, UNS R30008, UNS R30035, UNS R30605, and UNS R31537) |
| ISO 5838-1:2013 | Implants for surgery — Metallic skeletal pins and wires — Part 1: General requirements |
| DIN EN ISO 10993-6:2009-08 | BIOLOGICAL EVALUATION OF MEDICAL DEVICES - PART 6: TESTS FOR LOCAL EFFECTS AFTER IMPLANTATION (ISO 10993-6:2016) |
| ISO 9713:2002 | Neurosurgical implants — Self-closing intracranial aneurysm clips |
| ISO 10993-6:2016 | Biological evaluation of medical devices — Part 6: Tests for local effects after implantation |
| EN ISO 16061:2015 | Instrumentation for use in association with non-active surgical implants - General requirements (ISO 16061:2015) |
| DIN EN ISO 10993-6:2017-09 | BIOLOGICAL EVALUATION OF MEDICAL DEVICES - PART 6: TESTS FOR LOCAL EFFECTS AFTER IMPLANTATION (ISO 10993-6:2016) |
| UNE-EN ISO 16061:2015 | Instrumentation for use in association with non-active surgical implants - General requirements (ISO 16061:2015) |
| ISO 4967:2013 | Steel — Determination of content of non-metallic inclusions — Micrographic method using standard diagrams |
| ISO 6892-1:2016 | Metallic materials — Tensile testing — Part 1: Method of test at room temperature |
| ISO 643:2012 | Steels — Micrographic determination of the apparent grain size |
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