International safety notice
Kit de catéter balón intraaórtico Arrow FiberOptix y Arrow UltraFlex.
Spain / AEMPS · ESP · May 22, 2024
Key facts
| Title | Kit de catéter balón intraaórtico Arrow FiberOptix y Arrow UltraFlex. |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Kit de catéter balón intraaórtico Arrow FiberOptix y Arrow UltraFlex. |
| Manufacturer | Arrow International LLC (Subsidiary of Teleflex Incorporated), EEUU. |
| Models | 10801902172904, 18F23A0075, 18F22F0010, 18F23F0017, 18F23J0037, 18F24C0069, 18F23M0053, 18F23C0026, 18F22F0021, 18F23K0051, 250831, 240731 and 544 more |
| Event type | Safety Notice |
| Date | May 22, 2024 |
At a glance
- No Recall
- Yes 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