International safety notice
Dispositivo de oclusión intraaórtica IntraCludeTM, modelo ICF100
Spain / AEMPS · ESP · Jul 26, 2019
Key facts
| Title | Dispositivo de oclusión intraaórtica IntraCludeTM, modelo ICF100 |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Dispositivo de oclusión intraaórtica IntraCludeTM, modelo ICF100 |
| Manufacturer | Edwards Lifesciences LLC, EEUU |
| Models | 95475-206, 91.822.52.89, FCA-134, 46980, D-85716, 28022, ER23B, ER21B, 2019-413, IS19A, 92614, ICF100 and 1 more |
| Event type | Safety Notice |
| Date | Jul 26, 2019 |
At a glance
- No Recall
- Yes 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