International safety notice
Válvula Cardíaca Aórtica sin Sutura Perceval Plus: Modelo PVF-S, UDI-DI 08022057015365 Modelo PVF-M, UDI-DI 08022057015372 Modelo PVF-L, UDI-DI 08022057015389 Modelo PVF-XL, UDI-DI 08022057015396
Spain / AEMPS · ESP · Jan 15, 2024
Key facts
| Title | Válvula Cardíaca Aórtica sin Sutura Perceval Plus: Modelo PVF-S, UDI-DI 08022057015365 Modelo PVF-M, UDI-DI 08022057015372 Modelo PVF-L, UDI-DI 08022057015389 Modelo PVF-XL, UDI-DI 08022057015396 |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Válvula Cardíaca Aórtica sin Sutura Perceval Plus: Modelo PVF-S, UDI-DI 08022057015365 Modelo PVF-M, UDI-DI 08022057015372 Modelo PVF-L, UDI-DI 08022057015389 Modelo PVF-XL, UDI-DI 08022057015396 |
| Manufacturer | Corcym S.r.l., Italia |
| Models | PE9811A, PE6923A, PF0096A, PE7023A, PF0793A, PF1761A, PE6903C, PE6913A, PF2959A, PE7108A, PE7118A, PF2477A and 160 more |
| Event type | Safety Notice |
| Date | Jan 15, 2024 |
At a glance
- No Recall
- Yes 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