International safety notice
Urgent Field Safety Notice for CombiSet® TAVI, Hybrid Mediclin, Schrittmacherset by PAUL HARTMANN AG
Germany / BfArM · DEU · Oct 19, 2021
Key facts
| Title | Urgent Field Safety Notice for CombiSet® TAVI, Hybrid Mediclin, Schrittmacherset by PAUL HARTMANN AG |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | CombiSet® TAVI, Hybrid Mediclin, Schrittmacherset |
| Manufacturer | PAUL HARTMANN AG |
| Models | 2367881, 000641296, 100326291, 900118294, 2828332, 000106290, 100415292, 800323293, 15.10.2021, 2363042, 000342292, 000233293 and 70 more |
| Date | Oct 19, 2021 |
| 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