International safety notice
MobileDiagnost wDR, modelo R2 y referencias: 9890-010-89522, 712002, 712004, 712005, 712006 y 712007
Spain / AEMPS · ESP · Jun 3, 2024
Key facts
| Title | MobileDiagnost wDR, modelo R2 y referencias: 9890-010-89522, 712002, 712004, 712005, 712006 y 712007 |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | MobileDiagnost wDR, modelo R2 y referencias: 9890-010-89522, 712002, 712004, 712005, 712006 y 712007 |
| Manufacturer | Philips Medical Systems DMC GmbH, Alemania. |
| Models | SN19410102, 17200020, SN17200093, SN19410120, SN18200234, SN18200174, SN18200119, SN17200146, SN17200189, SN19410080, SN19300111, SN18200084 and 750 more |
| Event type | Safety Notice |
| Date | Jun 3, 2024 |
At a glance
- No Recall
- Yes Field safety notice
- 10–99 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