Quality
Recommendations of the Quality Committee
Here you will find the recommendations of the DGSV® Quality Committee, as published in „Zentralsterilization“. The recommendations are arranged in a ’new to old‘ order, which means that the most recent recommendations can always be found on this first page.
No results found
Keyword | Description | Link |
---|---|---|
FA-Q_EN_ZT_6_24_(36) | Risk management in the RUMED | Download |
FA-Q_EN_ZT_5_24_(56) | Reprocessing motor systems | Download |
FA-Q_EN_ZT_4_24_130 | Visual inspection, care and functional testing of surgical | Download |
FA-Q_EN_ZT_2_24_128 | Personnel Qualifications in the Reprocessing Unit forMP(Rumed) | Download |
FA-Q_EN_ZT_1_24_127 | Risk assessment of reprocessing-related products | Download |
FA-Q_EN_ZT_6_2023 | The use of ultrasonic cleaners for precleaning medical devices | Download |
FA-Q_EN_ZT_05_23_(85) | Recommendation on storage duration for sterile medical products | Download |
AK-Q_EN_Zt_04_2023_(33) | Mesh trays (and storage aids) and their implications | Download |
AK-Q_EN_Zt_42_03_(2023) | Use of test specimens to verify cleaning performance in the validation of cleaning-disinfection processes | Download |
AK-Q_EN_Zt_01_43 | Validation of steam sterilization processes in large | Download |
AK-Q_EN_ZT_01_125 | Comparison of sterile barrier systems | Download |
AK-Q_EN_Zt_06_124 | Is validation of processes in storage cabinets with controlled | Download |
AK-Q-Zt_123_04-2021 | Quality assurance in the RUMED through well-targeted | Download |
AK-Q_EN_Zt_02_122 | Job descriptions for employees | Download |
AK-Q_EN_Zt_01_121 | Quality assurance in the RUMED through well-targeted | Download |
AK-Q_EN_Zt_05_120 | Guide to compilation of standard operating procedures | Download |
AK-Q_EN_Zt_047_119 | Process chemicals in the medical device | Download |
AK-Q_EN_Zt_03_118 | Hygiene aspects when dealing with external persons | Download |
AK-Q_EN_Zt_02_117 | Transport between the site of use and reprocessing | Download |
AK-Q_EN_Zt_05_116 | Implications of MDR for the economic operator | Download |
AK-Q_EN_Zt_05_115 | Routine tests for monitoring the automated cleaning and disinfection process | Download |
AK-Q_EN_Zt_04_114 | Reprocessing of flexible endoscopes – Advantages and disadvantages of an AEMP close to or far from the examination site | Download |
AK-Q_EN_Zt_03_113 | Unambiguous traceability of medical device – Part 2 | Download |
AK-Q_EN_Zt_02_112 | Unambiguous traceability of medical device – Part 1 | Download |
AK-Q_EN_Zt_05_109 | Corrosion an underestimated risk | Download |
AK-Q_EN_Zt_04_108 | A Information to be provided by the medical device manufacturer – Part 2 | Download |
AK-Q_EN_Zt_06_108 | A Information to be provided by the medical device manufacturer – Part 2 – Update | Download |
AK-Q_EN_Zt_03_107 | A Information to be provided by the medical device manufacturer – Part 1 | Download |
AK-Q_EN_Zt__02_106 | No reprocessing of kidney bowls or wash bowls | Download |
AK-Q_EN_Zt_01_105 | Risk assessment and release of new medical devices | Download |
AK-Q_EN_03_2023_(85) | Recommendation for the storage period for sterile MP | Download |
AK-Q_EN_03_23_(42) | Use of test bodies to verify cleaning performance in the validation of cleaning-disinfection processes | Download |