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 · Feb 6, 2023
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 | 4056869063317ARTIS, 4056869046877ARTIS, 4056869046877, 28906, 2023PUEDE, AX002, 2022-571.LA, 88243, 4056869149325, 28022, 4056869063317, 2022-571 and 2 more |
| Event type | Safety Notice |
| Date | Feb 6, 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