International safety notice
Sensis UDI-DI 4056869010137; Sensis Vibe Hemo UDI-DI 4056869010199; Sensis Vibe Combo UDI-DI 4056869010205
Spain / AEMPS · ESP · Nov 24, 2022
Key facts
| Title | Sensis UDI-DI 4056869010137; Sensis Vibe Hemo UDI-DI 4056869010199; Sensis Vibe Combo UDI-DI 4056869010205 |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Sensis UDI-DI 4056869010137; Sensis Vibe Hemo UDI-DI 4056869010199; Sensis Vibe Combo UDI-DI 4056869010205 |
| Manufacturer | Siemens Healthcare GmbH, Alemania. |
| Models | 4056869010137, 4056869010199SENSIS, 2022-522, 4056869010205, 28022, DE-MF-000006122, 4056869010137SENSIS, 28906, 91.822.52.89, VD12A, AX057, AX058 and 4 more |
| Event type | Safety Notice |
| Date | Nov 24, 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