International safety notice
Urgent Field Safety Notice for Einwegschlauchsystem ohne BiCheck Flows by WEINMANN Emergency Medical Technology GmbH + Co. KG
Germany / BfArM · DEU · Jul 14, 2020
Key facts
| Title | Urgent Field Safety Notice for Einwegschlauchsystem ohne BiCheck Flows by WEINMANN Emergency Medical Technology GmbH + Co. KG |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Einwegschlauchsystem ohne BiCheck Flows |
| Manufacturer | WEINMANN Emergency Medical Technology GmbH + Co. KG |
| Models | 28183, 115967, 28695, 38144, 22770, 13485, 15840, 24558, 96-480, 47913245, DE35ZZZ00000353971, 15841 and 12 more |
| Date | Jul 14, 2020 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 10–99 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