International safety notice
Safety Information concerning all RT300 FES cycles with software versions 3.05.061 or earlier, Restorative Therapies
Germany / BfArM · DEU · Jan 26, 2012
Key facts
| Title | Safety Information concerning all RT300 FES cycles with software versions 3.05.061 or earlier, Restorative Therapies |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Safety Information concerning all RT300 FES cycles with software versions 3.05.061 or earlier, Restorative Therapies |
| Manufacturer | Safety Information concerning all RT300 FES cycles with software versions 3.05.061 or earlier, Restorative Therapies |
| Models | RT300, 3.05.061, 878-2466, 3.05.063, 609-9166, 21224 |
| Date | Jan 26, 2012 |
| 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