International safety notice
Aesculap AG
United Kingdom / MHRA · GBR · Sep 21, 2021
Key facts
| Title | Aesculap AG |
|---|---|
| Regulator | United Kingdom / MHRA |
| Country | GBR |
| Brand | BIPOLAR CUP TRIAL HEAD |
| Manufacturer | Aesculap AG |
| Models | 2259155, SA-DE13-M-5-4-02-000-5-A-DE, NF731, NF756, NG093, NF755, NG101, NG092, NG098, NF720, ID22.2, NF729 and 49 more |
| Event type | Safety Notice |
| Action type | Field safety notice |
| Date | Sep 21, 2021 |
| Regulator page | gov.uk |
At a glance
- No Recall
- Yes Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 Matching catalog numbers in FDA data
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