International safety notice
• Kit del reactivo STA – Deficient VIII (ref. 00725) • Kit del reactivo STA – InmunoDef VIII (ref. 00728) Utilizados con los analizadores de hemostasia de Stago: STA® Compact, STA® Compact Max, STA-R® Evolution y STA-R® Max.
Spain / AEMPS · ESP · Feb 28, 2020
Key facts
| Title | • Kit del reactivo STA – Deficient VIII (ref. 00725) • Kit del reactivo STA – InmunoDef VIII (ref. 00728) Utilizados con los analizadores de hemostasia de Stago: STA® Compact, STA® Compact Max, STA-R® Evolution y STA-R® Max. |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | • Kit del reactivo STA – Deficient VIII (ref. 00725) • Kit del reactivo STA – InmunoDef VIII (ref. 00728) Utilizados con los analizadores de hemostasia de Stago: STA® Compact, STA® Compact Max, STA-R® Evolution y STA-R® Max. |
| Manufacturer | Stago, Francia. |
| Models | 8012756, 0932131D, MS217, 0931633C, 517250_ES_V1, 110.05, 58069, 4.05.04, 110.06, 91.822.52.89, 08908, 517249_ES and 12 more |
| Event type | Safety Notice |
| Date | Feb 28, 2020 |
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