International safety notice
Corrective action of Roche for Cobas Amplicor HBV Monitor Test HBM Test Definition File
Germany / BfArM · DEU · May 11, 2005
Key facts
| Title | Corrective action of Roche for Cobas Amplicor HBV Monitor Test HBM Test Definition File |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Cobas Amplicor HBV Monitor Test HBM Test Definition File |
| Manufacturer | Corrective action of Roche for Cobas Amplicor HBV Monitor Test HBM Test Definition File |
| Models | V2.41, F08788, 10190, 04700295190.01, 36101, 00058004209.03, 00058003399-05, 5.6-FOLD |
| Date | May 11, 2005 |
| 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