International safety notice
Imtmedical AG
United Kingdom / MHRA · GBR · Oct 30, 2019
Key facts
| Title | Imtmedical AG |
|---|---|
| Regulator | United Kingdom / MHRA |
| Country | GBR |
| Brand | bellavista 1000 XX, bellavista 950 |
| Manufacturer | Imtmedical AG |
| Models | 301.100.100, 2019-001, 301.100.200, 301.100.060, MB100100, 1000E, 301.100.030, 2019001, 950.100.000, 301.100.000, 30.OCT.2019 |
| Event type | Safety Notice |
| Action type | Field safety notice |
| Medical specialty | General practice, Pharmacy |
| Date | Oct 30, 2019 |
| Regulator page | gov.uk |
At a glance
- No Recall
- Yes Field safety notice
- 10–99 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