NBR 15743-1 : 2017
Withdrawn
Withdrawn
A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.
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ORTHOPAEDIC IMPLANTS - TESTING SELECTION, INFORMATION AND REQUIREMENTS TO PROVIDE SAFETY AND EFFECTIVENESS - PART 1: GENERAL PROVISIONS
Amended by
Published date
28-07-2013
Publisher
Withdrawn date
19-12-2019
Superseded by
Sorry this product is not available in your region.
| Committee |
CB-026
|
| DevelopmentNote |
NEW CHILD AMD 1 2019 IS NOW ADDED
|
| DocumentType |
Standard
|
| ProductNote |
NEW CHILD AMD 1 2019 IS NOW ADDED
|
| PublisherName |
Brazilian Standards
|
| Status |
Withdrawn
|
| SupersededBy |
| NBR 15743-7 : 2017 | ORTHOPAEDIC IMPLANTS - TESTING SELECTION, INFORMATION AND REQUIREMENTS TO PROVIDE SAFETY AND EFFECTIVENESS - PART 7: IMPLANTS MANUFACTURED OF ABSORBABLE POLYMERS |
| NBR 15743-10 : 2017 | ORTHOPAEDIC IMPLANTS - TESTING SELECTION, INFORMATION AND REQUIREMENTS TO PROVIDE SAFETY AND EFFECTIVENESS - PART 10: BONE ANCHORING SYSTEMS |
| NBR 15743-9 : 2017 | ORTHOPAEDIC IMPLANTS - TESTING SELECTION, INFORMATION AND REQUIREMENTS TO PROVIDE SAFETY AND EFFECTIVENESS - PART 9: COMPATIBILITY IN MAGNETIC RESONANCE ENVIRONMENT |
| NBR 15743-4 : 2017 | ORTHOPAEDIC IMPLANTS -TESTING SELECTION, INFORMATION AND REQUIREMENTS TO PROVIDE SAFETY AND EFFECTIVENESS - PART 4: TOTAL INTERVERTEBRAL DISC PROSTHESIS |
| NBR 15743-2 : 2017 | ORTHOPAEDIC IMPLANTS - TESTING SELECTION, INFORMATION AND REQUIREMENTS TO PROVIDE SAFETY AND EFFECTIVENESS - PART 2: IMPLANT WITH COATING |
| NBR 15743-3 : 2017 | ORTHOPAEDIC IMPLANTS -TESTING SELECTION, INFORMATION AND REQUIREMENTS TO PROVIDE SAFETY AND EFFECTIVENESS - PART 3: DEVICES FOR ARTHRODESIS OF VERTEBRAL BODIES |
| NBR 16465 : 2016 | IMPLANTS FOR SURGERY - REQUIREMENTS FOR PACKAGING AND PACKING OF PRODUCT FOR SUPPLY |
| NBR ISO 11607-1 : 2013 | PACKAGING FOR TERMINALLY STERILIZED MEDICAL DEVICES - PART 1: REQUIREMENTS FOR MATERIAL, STERILE BARRIER SYSTEMS AND PACKAGING SYSTEMS |
| ISO/TR 14283:2004 | Implants for surgery — Fundamental principles |
| NBR ISO 14971 : 2009 | MEDICAL DEVICES - APPLICATION OF RISK MANAGEMENT TO MEDICAL DEVICES |
| NBR ISO 11607-2 : 2013 | PACKAGING FOR TERMINALLY STERILIZED MEDICAL DEVICES - PART 2: VALIDATION REQUIREMENTS FOR FORMING, SEALING AND ASSEMBLY PROCESSES |
| NBR ISO 10993-1 : 2013 | BIOLOGICAL EVALUATION OF MEDICAL DEVICES - PART 1: EVALUATION AND TESTING WITHIN A RISK MANAGEMENT PROCESS |
| ISO 14155:2011 | Clinical investigation of medical devices for human subjects — Good clinical practice |
| NBR 15678 : 2011 | ORTHOPEDICS IMPLANTS - SPECIFICATION FOR RIGID POLYURETHANE FOAM FOR USE AS A STANDARD MATERIAL FOR TESTING ORTHOPEDIC IMPLANTS AND INSTRUMENTS |
| NBR ISO 14630 : 2013 ERRATA 1 2013 | NON-ACTIVE SURGICAL IMPLANTS - GENERAL REQUIREMENTS |
Summarise
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