International safety notice
- Sensis UDI-DI: 4056869010137 - Sensis vibe Hemo UDI-DI: 4056869010199 - Sensis Vibe combo UDI-DI: 4056869010205
Spain / AEMPS · ESP · Dec 22, 2023
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 | AX010, 2023-606, AX038, 28022, SOFTWAREVD15B, 100720, 4056869010205, 4056869010199SENSIS, 28043, 4056869010137, VD15B, 4056869010137SENSIS and 2 more |
| Event type | Safety Notice |
| Date | Dec 22, 2023 |
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