International safety notice
Analizador de grupos sanguíneos IH-1000: - Referencia 001000, UDI-DI: 07611969205516 - Refererencia 001000RECOND, UDI-DI: 03610522063680
Spain / AEMPS · ESP · Feb 15, 2023
Key facts
| Title | Analizador de grupos sanguíneos IH-1000: - Referencia 001000, UDI-DI: 07611969205516 - Refererencia 001000RECOND, UDI-DI: 03610522063680 |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Analizador de grupos sanguíneos IH-1000: - Referencia 001000, UDI-DI: 07611969205516 - Refererencia 001000RECOND, UDI-DI: 03610522063680 |
| Manufacturer | DiaMed GmbH, Suiza |
| Models | PR80E, SOFTWARE04.08.11, 89642, 03610522063680, PR80H, PR70H, PR80B, PR80I, 07611969205516, 91.822.52.89, 6.1.4, PR70B and 21 more |
| Event type | Safety Notice |
| Date | Feb 15, 2023 |
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