International safety notice
Kit de reactivos: - Devyser BRCA, lote 24J211, UDI-DI 07350040631775 - Devyser CFTR, lote 24F999, UDI-DI 07350040631805 - Devyser HBOC, lote 24B338, UDI-DI 07350040631638 - Devyser Talasemia, lote 24L554, UDI-DI 07350040631591
Spain / AEMPS · ESP · Mar 7, 2025
Key facts
| Title | Kit de reactivos: - Devyser BRCA, lote 24J211, UDI-DI 07350040631775 - Devyser CFTR, lote 24F999, UDI-DI 07350040631805 - Devyser HBOC, lote 24B338, UDI-DI 07350040631638 - Devyser Talasemia, lote 24L554, UDI-DI 07350040631591 |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Kit de reactivos: - Devyser BRCA, lote 24J211, UDI-DI 07350040631775 - Devyser CFTR, lote 24F999, UDI-DI 07350040631805 - Devyser HBOC, lote 24B338, UDI-DI 07350040631638 - Devyser Talasemia, lote 24L554, UDI-DI 07350040631591 |
| Manufacturer | Devyser AB, Suecia. |
| Models | 24J211, 24B338, 07350040631775, 24F999, 07350040631638, 24L554, 07350040631805, 07350040631591 |
| Event type | Safety Notice |
| Date | Mar 7, 2025 |
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