International safety notice
Urgent Field Safety Notice for Atellica COAG 360 System by Siemens Healthcare Diagnostics Products GmbH
Germany / BfArM · DEU · Dec 22, 2020
Key facts
| Title | Urgent Field Safety Notice for Atellica COAG 360 System by Siemens Healthcare Diagnostics Products GmbH |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Atellica COAG 360 System |
| Manufacturer | Siemens Healthcare Diagnostics Products GmbH |
| Models | 27000, 13000, 71001, 15010, 14200, 11468626, 33100, 15000, 71000, 26100, 13100, 27100 and 16 more |
| Date | Dec 22, 2020 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1,000+ Matching device models in FDA data
- 1,000+ 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