International safety notice
Urgent Field Safety Notice for Revas Veno-venöse Dual Lumen Kanüle Rheopax by free life medical GmbH
Germany / BfArM · DEU · Apr 11, 2019
Key facts
| Title | Urgent Field Safety Notice for Revas Veno-venöse Dual Lumen Kanüle Rheopax by free life medical GmbH |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Revas Veno-venöse Dual Lumen Kanüle Rheopax |
| Manufacturer | free life medical GmbH |
| Models | K07V02F02, 00-90, 2405-41, VV27R, 01.09.2018, V19B22R, V20B20, V20B20R, 03.2018, VV19R, OB26R, 52080 and 7 more |
| Date | Apr 11, 2019 |
| 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