International safety notice
• Guía de catéter hidrofílico HYBRID • Kits de microcatéter SONIC con la Guía de catéter hidrofílico HYBRID
Spain / AEMPS · ESP · Nov 15, 2023
Key facts
| Title | • Guía de catéter hidrofílico HYBRID • Kits de microcatéter SONIC con la Guía de catéter hidrofílico HYBRID |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | • Guía de catéter hidrofílico HYBRID • Kits de microcatéter SONIC con la Guía de catéter hidrofílico HYBRID |
| Manufacturer | BALT EXTRUSION SAS. Francia. |
| Models | 00520500, 20231011_HYBRID, 00506369, 03700481334430, HYBRID007D-KIT, 33.1.39.89.46.41, HYBRID007D, 95160, 33.1.34.17.03.46, 03700481334386, 00506801, HYBRID008J and 24 more |
| Event type | Safety Notice |
| Date | Nov 15, 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