International safety notice
CombiDiagnost R90 (números de modelo: 709030 y 709031) y ProxiDiagnost N90 (número de modelo: 706100)
Spain / AEMPS · ESP · Nov 11, 2021
Key facts
| Title | CombiDiagnost R90 (números de modelo: 709030 y 709031) y ProxiDiagnost N90 (número de modelo: 706100) |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | CombiDiagnost R90 (números de modelo: 709030 y 709031) y ProxiDiagnost N90 (número de modelo: 706100) |
| Manufacturer | Philips Medical Systems DMC GmbH, Alemania. |
| Models | 28022, 709031, 28050, 73816, 21CFR, 2021-PD-DXR-012_70900056, 91.822.52.89, 709030, 1020.30, 706100, 2021-615, 70900056 and 1 more |
| Event type | Safety Notice |
| Date | Nov 11, 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