International safety notice
Sistemas Sensis, referencia 10764561, Sensis Vibe Combo, referencia 11007642 y Sensis Vibe Hemo, referencia 11007641.
Spain / AEMPS · ESP · Nov 10, 2021
Key facts
| Title | Sistemas Sensis, referencia 10764561, Sensis Vibe Combo, referencia 11007642 y Sensis Vibe Hemo, referencia 11007641. |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Sistemas Sensis, referencia 10764561, Sensis Vibe Combo, referencia 11007642 y Sensis Vibe Hemo, referencia 11007641. |
| Manufacturer | Siemens Healthcare GmbH, Alemania. |
| Models | 11007641, 11007642.SENSIS, 73134, 10764561, 10764561.SENSIS, AX067, AX066, 11007642, 28022, 2021-605, 28906, 91.822.52.89 |
| Event type | Safety Notice |
| Date | Nov 10, 2021 |
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