International safety notice
Balt Extrusion SAS HYBRID guidewire - tagasikutsumine, vale pakendi märgistus
Estonia / EMDDB · EST · Oct 1, 2023
Key facts
| Title | Balt Extrusion SAS HYBRID guidewire - tagasikutsumine, vale pakendi märgistus |
|---|---|
| Regulator | Estonia / EMDDB |
| Country | EST |
| Brand | Balt Extrusion SAS HYBRID guidewire |
| Manufacturer | BALT EXTRUSION SAS HYBRID GUIDEWIRE |
| Models | HYBRID008J, 00513093, 03700781338261, 20231011_, HYBRID007D, 00506369, SONIC1.2F25, 00513550, SONIC1.2F15, 03700481334331, 00840303702108, HYBRID008D and 18 more |
| Date | Oct 1, 2023 |
| Regulator page | terviseamet.ee |
At a glance
- No Recall
- No 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