International safety notice
OmniDiagnost Eleva
Swiss / SwissMedic · CHE · Mar 27, 2019
Key facts
| Title | OmniDiagnost Eleva |
|---|---|
| Regulator | Swiss / SwissMedic |
| Country | CHE |
| Brand | OmniDiagnost Eleva |
| Manufacturer | Philips Medical Systems Nederland BV |
| Models | 708032, 708037MultiDiagnost, 708037, 708035MultiDiagnost, 708032UroDiagnost, 708035, 708034MultiDiagnost, 708028, 70802870859708023708024OmniDiagnost, 708032Urodiagnost, 70859, 708036 and 12 more |
| Event type | Safety Notice |
| Date | Mar 27, 2019 |
| Regulator page | fsca.swissmedic.ch |
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