ISO 16054:2000
Withdrawn
Withdrawn
A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.
View Superseded by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 Minimum data sets for surgical implants
Available format(s)
PDF 1 User , PDF 3 Users , PDF 5 Users , PDF 9 Users
Withdrawn date
06-11-2019
Superseded by
Language(s)
English, French
Published date
21-12-2000
Important note : All end users must be registered with an Account prior to user licenses being assigned.| DevelopmentNote |
DRAFT ISO/DIS 16054 is also available for this standard. (10/2017)
|
| DocumentType |
Standard
|
| Pages |
4
|
| PublisherName |
International Organization for Standardization
|
| Status |
Withdrawn
|
| SupersededBy |
| Standards | Relationship |
| DIN EN ISO 16054:2019-10 | Identical |
| NBN EN ISO 16054 : 2002 | Identical |
| PN EN ISO 16054 : 2003 | Identical |
| UNI EN ISO 16054:2019 | Identical |
| I.S. EN ISO 16054:2002 | Identical |
| NF EN ISO 16054 : 2002 | Identical |
| BS ISO 16054 : 2000 AMD 14017 | Identical |
| DIN EN ISO 16054:2002-09 | Identical |
| NEN EN ISO 16054 : 2002 | Identical |
| I.S. EN ISO 16054:2019 | Identical |
| EN ISO 16054:2002 | Identical |
| ONORM EN ISO 16054 : 2002 | Identical |
| NEN ISO 16054 : 2001 | Identical |
| GOST R ISO 16054 : 2013 | Identical |
| UNI EN ISO 16054 : 2002 | Identical |
| UNE-EN ISO 16054:2002 | Identical |
| BS EN ISO 16054:2002 | Identical |
| SN EN ISO 16054 : 2002 | Identical |
| DD ISO/TS 12417:2011 | Cardiovascular implants and extracorporeal systems. Vascular device-drug combination products |
| DIN EN ISO 12417-1:2016-02 | Cardiovascular implants and extracorporeal systems - Vascular device-drug combination products - Part 1: General requirements (ISO 12417-1:2015) |
| I.S. EN ISO 14607:2009 | NON-ACTIVE SURGICAL IMPLANTS - MAMMARY IMPLANTS - PARTICULAR REQUIREMENTS (ISO 14607:2018) |
| DIN EN ISO 14607:2009-08 | NON-ACTIVE SURGICAL IMPLANTS - MAMMARY IMPLANTS - PARTICULAR REQUIREMENTS |
| ISO 14607:2007 | Non-active surgical implants Mammary implants Particular requirements |
| ISO/TS 12417:2011 | Cardiovascular implants and extracorporeal systems Vascular device-drug combination products |
| 14/30251609 DC : 0 | BS EN ISO 12417-1 - CARDIOVASCULAR IMPLANTS AND EXTRACORPOREAL SYSTEMS - VASCULAR DEVICE-DRUG COMBINATION PRODUCTS - PART 1: GENERAL REQUIREMENTS |
| 13/30278952 DC : 0 | BS EN 16372 - AESTHETIC SURGERY AND AESTHETIC NON-SURGICAL MEDICAL SERVICES |
| AAMI ISO 12417-1 : 2015 | CARDIOVASCULAR IMPLANTS AND EXTRACORPOREAL SYSTEMS - VASCULAR DEVICE-DRUG COMBINATION PRODUCTS - PART 1: GENERAL REQUIREMENTS |
| S.R. CEN/CLC/TR 14060:2014 | MEDICAL DEVICE TRACEABILITY ENABLED BY UNIQUE DEVICE IDENTIFICATION (UDI) |
| BS EN ISO 14607:2009 | Non-active surgical implants. Mammary implants. Particular requirements |
| UNI EN ISO 14607 : 2009 | NON-ACTIVE SURGICAL IMPLANTS - MAMMARY IMPLANTS - PARTICULAR REQUIREMENTS |
| 15/30317874 DC : 0 | BS EN 16844 - AESTHETIC MEDICINE SERVICES - NON-SURGICAL MEDICAL PROCEDURES |
| BS EN ISO 12417-1:2015 | Cardiovascular implants and extracorporeal systems. Vascular device-drug combination products General requirements |
| UNE-EN 16372:2015 | Aesthetic surgery services |
| 12/30254927 DC : 0 | BS EN 16372 - AESTHETIC SURGERY SERVICES |
| I.S. EN ISO 12417-1:2015 | CARDIOVASCULAR IMPLANTS AND EXTRACORPOREAL SYSTEMS - VASCULAR DEVICE-DRUG COMBINATION PRODUCTS - PART 1: GENERAL REQUIREMENTS (ISO 12417-1:2015) |
| I.S. EN 16372:2014 | AESTHETIC SURGERY SERVICES |
| CEN/CLC/TR 14060:2014 | Medical device traceability enabled by unique device identification (UDI) |
| EN 16844:2017 | Aesthetic medicine services - Non-surgical medical treatments |
| I.S. EN 16844:2017 | AESTHETIC MEDICINE SERVICES - NON-SURGICAL MEDICAL PROCEDURES |
| UNE-EN ISO 12417-1:2016 | Cardiovascular implants and extracorporeal systems - Vascular device-drug combination products - Part 1: General requirements (ISO 12417-1:2015) |
| ISO/TR 12417-2:2017 | Cardiovascular implants and extracorporeal systems — Vascular device-drug combination products — Part 2: Local regulatory information |
| EN ISO 14607:2018 | Non-active surgical implants - Mammary implants - Particular requirements (ISO 14607:2018, Corrected version 2018-08) |
| ISO 12417-1:2015 | Cardiovascular implants and extracorporeal systems — Vascular device-drug combination products — Part 1: General requirements |
| EN 16372:2014 | Aesthetic surgery services |
| EN ISO 12417-1:2015 | Cardiovascular implants and extracorporeal systems - Vascular device-drug combination products - Part 1: General requirements (ISO 12417-1:2015) |
| AAMI ISO TIR 12417 : 2011 | CARDIOVASCULAR IMPLANTS AND EXTRACORPOREAL SYSTEMS - VASCULAR DEVICE-DRUG COMBINATION PRODUCTS |
| BS EN 16372:2014 | Aesthetic surgery services |
| I.S. EN 16844:2017+A2:2019 | Aesthetic medicine services - Non-surgical medical treatments |
| BS EN 16844 : 2017 | AESTHETIC MEDICINE SERVICES - NON-SURGICAL MEDICAL TREATMENTS |
| ISO 13485:2016 | Medical devices Quality management systems Requirements for regulatory purposes |
| ISO 8402:1994 | Quality management and quality assurance — Vocabulary |
| EN 800 : 1995 | BAR CODING - SYMBOLOGY SPECIFICATIONS - "CODE 39" |
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