International safety notice
Analizador ABL700 Analizadores ABL800 Basic, UDI-DI básico 57006900036MW y ABL8XX FLEX, UDI-DI básico 57006900037MY
Spain / AEMPS · ESP · May 31, 2022
Key facts
| Title | Analizador ABL700 Analizadores ABL800 Basic, UDI-DI básico 57006900036MW y ABL8XX FLEX, UDI-DI básico 57006900037MY |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Analizador ABL700 Analizadores ABL800 Basic, UDI-DI básico 57006900036MW y ABL8XX FLEX, UDI-DI básico 57006900037MY |
| Manufacturer | Radiometer Medical ApS. Dinamarca. |
| Models | 2022-260, ABL8XX, ABL800, 79697, ABL700NOTA, ABL700, ABL700ANALIZADORES, 57006900036MW, 91.822.52.89, V6.19, 28108, 57006900037MY and 2 more |
| Event type | Safety Notice |
| Date | May 31, 2022 |
At a glance
- No Recall
- Yes Field safety notice
- 1–9 Matching device models in FDA data
- 1–9 Matching catalog numbers 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