International safety notice
Mesa QF VE en los sistemas:ARTIS pheno, UDI-DI 4056869046877 ARTIS icono biplane, UDI-DI 4056869063317 ARTIS icono floor, UDI-DI 4056869149325
Spain / AEMPS · ESP · Dec 23, 2022
Key facts
| Title | Mesa QF VE en los sistemas:ARTIS pheno, UDI-DI 4056869046877 ARTIS icono biplane, UDI-DI 4056869063317 ARTIS icono floor, UDI-DI 4056869149325 |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Mesa QF VE en los sistemas:ARTIS pheno, UDI-DI 4056869046877 ARTIS icono biplane, UDI-DI 4056869063317 ARTIS icono floor, UDI-DI 4056869149325 |
| Manufacturer | Siemens Healthcare GmbH, Alemania. |
| Models | 4056869149325, 2022PUEDE, 4056869063317ARTIS, 2022-571, 88243, 4056869046877, 28906, 4056869046877ARTIS, 4056869063317, AX047, 91.822.52.89, 28022 and 1 more |
| Event type | Safety Notice |
| Date | Dec 23, 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