International safety notice
Additional Information concerning the corrective action for AMH Gen II Elisa, Beckman Coulter
Germany / BfArM · DEU · Jul 25, 2013
Key facts
| Title | Additional Information concerning the corrective action for AMH Gen II Elisa, Beckman Coulter |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | AMH Gen II Elisa, Beckman Coulter |
| Manufacturer | Additional Information concerning the corrective action for AMH Gen II Elisa, Beckman Coulter |
| Models | 326119, FSN-20434-2, FSN-20434, A92268D, A56021, A79765 |
| Date | Jul 25, 2013 |
| 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