International safety notice
Corrective action for the Pulsar-18 and Pulsar-35 peripheral self-expanding Nitinol stent systems, Biotronik AG
Germany / BfArM · DEU · Jun 2, 2015
Key facts
| Title | Corrective action for the Pulsar-18 and Pulsar-35 peripheral self-expanding Nitinol stent systems, Biotronik AG |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the Pulsar-18 and Pulsar-35 peripheral self-expanding Nitinol stent systems, Biotronik AG |
| Manufacturer | Corrective action for the Pulsar-18 and Pulsar-35 peripheral self-expanding Nitinol stent systems, Biotronik AG |
| Models | 0413XXXX, 0813XXXX, 379921, 12XXXX, 0913XXXX, 379946, 0614XXXX, 379926, 0812XXXX, 13XXXX, 366812, 366822 and 25 more |
| Date | Jun 2, 2015 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No 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