International safety notice
Urgent Field Safety Notice for VITELENE PE-INSERT ID 22,2, 28, 32 und 36 MM by Aesculap AG
Germany / BfArM · DEU · Apr 19, 2024
Key facts
| Title | Urgent Field Safety Notice for VITELENE PE-INSERT ID 22,2, 28, 32 und 36 MM by Aesculap AG |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | VITELENE PE-INSERT ID 22,2, 28, 32 und 36 MM |
| Manufacturer | Aesculap AG |
| Models | AUF3ENPFANNE, NV315E, BEH6RDE, •U•.1-·, MAL3NAHME, 04.2019-04.2024, 52883304, 403923900000168536, 4915118322990, ANLAN9EN, 288I2JTJ•T9FIGURE, 17.04.2024 and 18 more |
| Date | Apr 19, 2024 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models in FDA data
- 1–9 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