Reprocessing
According to the Medizinprodukte-Betreiberverordnung – MPBetreibV (§ 8 Abs. 2) a “proper reprocessing […] is assumed if the Joint Recommendation of the Commission for Hospital Hygiene and the Prevention of Infection at the Robert Koch Institute and the Federal Institute for Drugs and Medical Products concerning Hygiene Requirements when Reprocessing Medical Devices is observed”. 1)
Acronym | Name |
NA 014-00-21-02 AK | |
NA 014-00-23 AA | |
NA 027-02-01 AA | |
NA 063-01-07 AA | |
NA 063-04-01 AA | |
NA 063-04-02 AA | |
NA 063-04-03 AA | |
NA 063-04-04 AA | |
NA 063-04-08 AA | |
NA 063-04-09 AA |
1) MDI, Prof. Dr. Volker Großkopf and Dr. Christian Jäkel, S. 2
