International safety notice
Recall of the 200 mm sinus-SuperFlex-635 self-expanding nitinol stent system, optimed Medizinische Instrumente GmbH
Germany / BfArM · DEU · Jul 27, 2015
Key facts
| Title | Recall of the 200 mm sinus-SuperFlex-635 self-expanding nitinol stent system, optimed Medizinische Instrumente GmbH |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of the 200 mm sinus-SuperFlex-635 self-expanding nitinol stent system, optimed Medizinische Instrumente GmbH |
| Manufacturer | Recall of the 200 mm sinus-SuperFlex-635 self-expanding nitinol stent system, optimed Medizinische Instrumente GmbH |
| Models | 15-028, 8607-7200, 07243, 8607-6200, 7633-584, 76275, 8606-6200, 7X200, 22.07, 6X200, SUPERFLEX-635, SINUS-SUPERFLEX-635 and 3 more |
| Date | Jul 27, 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