International safety notice
Additional Instruction for Use for the Edi catheter, Maquet Critical Care AB
Germany / BfArM · DEU · Mar 17, 2014
Key facts
| Title | Additional Instruction for Use for the Edi catheter, Maquet Critical Care AB |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the Edi catheter, Maquet Critical Care AB |
| Manufacturer | Additional Instruction for Use for the Edi catheter, Maquet Critical Care AB |
| Models | MM_0191-05, 6685782, 6685780, 6685777, 6685775, 6685790, 6685787 |
| Date | Mar 17, 2014 |
| 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