International safety notice
Updated Instructions for Use for Thermablate Endometrial Ablation System (EAS), Idoman Teoranta
Germany / BfArM · DEU · May 30, 2014
Key facts
| Title | Updated Instructions for Use for Thermablate Endometrial Ablation System (EAS), Idoman Teoranta |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Thermablate Endometrial Ablation System (EAS), Idoman Teoranta |
| Manufacturer | Updated Instructions for Use for Thermablate Endometrial Ablation System (EAS), Idoman Teoranta |
| Models | 21004, 0.5CM, 2343932, 9544726, 9544725, 22101, 355594, LS2101 |
| Date | May 30, 2014 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 10–99 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