International safety notice
MEDISA Automated Endoscope Reprocessor (AER)
Swiss / SwissMedic · CHE · Mar 29, 2025
Key facts
| Title | MEDISA Automated Endoscope Reprocessor (AER) |
|---|---|
| Regulator | Swiss / SwissMedic |
| Country | CHE |
| Brand | MEDISA Automated Endoscope Reprocessor (AER) |
| Manufacturer | Cantel Medical (Italy) S.r.l. |
| Models | 8011517EWD002GL, 8011517EWD001GJ |
| Event type | Safety Notice |
| Date | Mar 29, 2025 |
| Regulator page | fsca.swissmedic.ch |
At a glance
- No Recall
- Yes Field safety notice
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About International device safety notices
Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.
Source: National medical device regulators (as listed), compiled by Orca1