International safety notice
Final Information concerning the OptonPro device for laser therapy, Zimmer MedizinSysteme GmbH
Germany / BfArM · DEU · Aug 25, 2014
Key facts
| Title | Final Information concerning the OptonPro device for laser therapy, Zimmer MedizinSysteme GmbH |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | laser therapy, Zimmer MedizinSysteme GmbH |
| Manufacturer | Final Information concerning the OptonPro device for laser therapy, Zimmer MedizinSysteme GmbH |
| Models | 788005, 65071610, 30.07.2014, 30.07.2013, 1606788005, 130856191, 97610, 190437, 89231, FF630, 9761-162, 74010185 and 2 more |
| Date | Aug 25, 2014 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models 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