International safety notice
Siemens Healthcare
United Kingdom / MHRA · GBR · Feb 25, 2019
Key facts
| Title | Siemens Healthcare |
|---|---|
| Regulator | United Kingdom / MHRA |
| Country | GBR |
| Brand | UROSKOP OMNIA and UROSKOP OMNIA MAX |
| Manufacturer | Siemens Healthcare |
| Models | 10094910, 64872105, XP006, 91301, 10762473, NO.10999410, 10999410, 213821, XP004, 18-4084 |
| Event type | Safety Notice |
| Action type | Field safety notice |
| Date | Feb 25, 2019 |
| Regulator page | gov.uk |
At a glance
- No Recall
- Yes Field safety notice
- 1–9 Matching device models 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