International safety notice
Urgent Safety Notice for the IntraClude™ intra-aortic occlusion device Model ICF100, Edwards Lifesciences
Germany / BfArM · DEU · Jun 1, 2015
Key facts
| Title | Urgent Safety Notice for the IntraClude™ intra-aortic occlusion device Model ICF100, Edwards Lifesciences |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the IntraClude™ intra-aortic occlusion device Model ICF100, Edwards Lifesciences |
| Manufacturer | Urgent Safety Notice for the IntraClude™ intra-aortic occlusion device Model ICF100, Edwards Lifesciences |
| Models | ICF100, FCA-61 |
| Date | Jun 1, 2015 |
| 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