VDI 5700 Blatt 2:2017-06
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
View Superseded by
Reprocessing hazards - Risk management in reprocessing of medical devices - Trainings
Hardcopy , PDF
German - English
01-06-2017
03-03-2023
Preliminary note
Introduction
1 Scope
2 Normative references
3 Terms and definitions
4 Abbreviations
5 Training categories and training
prerequisites
6 Qualification of experts
7 Quality characteristics of training
courses and instructions
8 Training subjects and contents
9 Examinations
10 Certificates
Annex A - Training subjects and contents
Annex B - Certificate template
Bibliography
Applies to courses for further training of staff in the field of reprocessing of medical devices (process-related training) and of staff of medical devices manufacturers, particularly developers (device-related training).
| DocumentType |
Standard
|
| Pages |
16
|
| PublisherName |
Verlag des Vereins Deutscher Ingenieure
|
| Status |
Superseded
|
| SupersededBy | |
| Supersedes |
| DIN EN ISO 17664:2016-06 (Draft) | PROCESSING OF HEALTH CARE PRODUCTS - INFORMATION TO BE PROVIDED BY THE MEDICAL DEVICE MANUFACTURER FOR THE PROCESSING OF MEDICAL DEVICES (ISO 17664:2017) |
| DIN EN ISO 14971:2013-04 | MEDICAL DEVICES - APPLICATION OF RISK MANAGEMENT TO MEDICAL DEVICES (ISO 14971:2007) |
| VDI 5700 Blatt 1:2015-04 | Reprocessing hazards - Risk management in reprocessing of medical devices - Measures for risk control |
| VDI 1000:2017-02 | VDI Standardisation Work - Principles and procedures |
| ISO 10993-1:2009 | Biological evaluation of medical devices — Part 1: Evaluation and testing within a risk management process |
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