International safety notice
Philips CombiDiagnost R90 ja ProxiDiagnost N90 - potentsiaalne komponendi kahjustus ja laua seiskumine
Estonia / EMDDB · EST · Apr 1, 2023
Key facts
| Title | Philips CombiDiagnost R90 ja ProxiDiagnost N90 - potentsiaalne komponendi kahjustus ja laua seiskumine |
|---|---|
| Regulator | Estonia / EMDDB |
| Country | EST |
| Brand | Philips CombiDiagnost R90 ja ProxiDiagnost N90 |
| Manufacturer | PHILIPS COMBIDIAGNOST R90 JA PROXIDIAGNOST N90 |
| Models | 0088483808561921, 709030709031, 10001082, 10001020, 10000046, 10000135, 20000089, 20000081, 10001060, SN19000026, 20000071, 20000086 and 567 more |
| Date | Apr 1, 2023 |
| Regulator page | terviseamet.ee |
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