International safety notice
Guía hidrofílica HYBRID12D300. UDI-DI: 03700481334447. (fabricadas antes de junio de 2023)
Spain / AEMPS · ESP · Sep 22, 2023
Key facts
| Title | Guía hidrofílica HYBRID12D300. UDI-DI: 03700481334447. (fabricadas antes de junio de 2023) |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Guía hidrofílica HYBRID12D300. UDI-DI: 03700481334447. (fabricadas antes de junio de 2023) |
| Manufacturer | BALT EXTRUSION SAS, Francia. |
| Models | 20230719, 28022, 08011, 00467647, 91.822.52.89, HYBRID12D300, 95160, 33.1.34.17.03.46, 00471945, FSN20230719_HYBRID, 03700481334447, 97791 and 2 more |
| Event type | Safety Notice |
| Date | Sep 22, 2023 |
At a glance
- No Recall
- Yes Field safety notice
- 1–9 Matching device models 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