International safety notice
Follow-up information for ARCHITECT c8000, Abbott
Germany / BfArM · DEU · Jul 2, 2008
Key facts
| Title | Follow-up information for ARCHITECT c8000, Abbott |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | ARCHITECT c8000, Abbott |
| Manufacturer | Follow-up information for ARCHITECT c8000, Abbott |
| Models | FA23MAY2008, 60064-6081, 05F48-17, CI8200, C8000, 05F48-14, FA11JUN2008, 05F48-21, 3.12…, 05F48-20, 7-201738-02, 05F48-18 and 11 more |
| Date | Jul 2, 2008 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
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