International safety notice
Safety Information for AMPLILINK 3.2.2 software, Roche Diagnostics
Germany / BfArM · DEU · May 18, 2009
Key facts
| Title | Safety Information for AMPLILINK 3.2.2 software , Roche Diagnostics |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | AMPLILINK 3.2.2 software , Roche Diagnostics |
| Manufacturer | Safety Information for AMPLILINK 3.2.2 software , Roche Diagnostics |
| Models | 3203PM, NHWI7.0209, E83123WCT, EHCMCÅP48, 2MM0311, H3VÜ2CL.T9, 00811144, K101ARM, 39152, 2IW2CB1211HHO, 3.2.2, HODCÅP4811 and 24 more |
| Date | May 18, 2009 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 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