International safety notice
Corrective action of BEP 2000 / BEP 2000 Advance System, Dade Behring
Germany / BfArM · DEU · Feb 16, 2005
Key facts
| Title | Corrective action of BEP 2000 / BEP 2000 Advance System, Dade Behring |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Corrective action of BEP 2000 / BEP 2000 Advance System, Dade Behring |
| Manufacturer | Corrective action of BEP 2000 / BEP 2000 Advance System, Dade Behring |
| Models | 35001, 0&421, 66064, 496421-39-3070, Z4-FEB-2ØØS, 2000Ö, 436421334372, FRAN8FVNMALN, 39-5-405, GS241ECNQFT, 34-FEE-2ÜÜS, FRANKIUR4NIEJN and 4 more |
| Date | Feb 16, 2005 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 100–999 Matching device models in FDA data
- 10–99 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