International safety notice
Urgent Field Safety Notice for CombiDiagnost R90/ProxiDiagnost N90 by Philips Medical Systems DMC GmbH
Germany / BfArM · DEU · Apr 26, 2023
Key facts
| Title | Urgent Field Safety Notice for CombiDiagnost R90/ProxiDiagnost N90 by Philips Medical Systems DMC GmbH |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | CombiDiagnost R90/ProxiDiagnost N90 |
| Manufacturer | Philips Medical Systems DMC GmbH |
| Models | SN18000046, 10000072, 10001099, 10001048, 20000086, 10000121, SN17000135, 10000065, SN16000004, SN18000039, 10001014, 10001009 and 554 more |
| Date | Apr 26, 2023 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 100–999 Matching device models in FDA data
- 10–99 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