International safety notice
Shenzhen Mindray Bio-medical:The BeneVision N22 and N19 patient monitors
United Kingdom / MHRA · GBR · Jun 1, 2016
Key facts
| Title | Shenzhen Mindray Bio-medical:The BeneVision N22 and N19 patient monitors |
|---|---|
| Regulator | United Kingdom / MHRA |
| Country | GBR |
| Brand | Shenzhen Mindray Bio-medical:The BeneVision N22 and N19 patient monitors |
| Manufacturer | Shenzhen Mindray Bio-medical:The BeneVision N22 and N19 patient monitors |
| Event type | Safety Notice |
| Action type | Field safety notice |
| Date | Jun 1, 2016 |
| Regulator page | gov.uk |
At a glance
- No Recall
- Yes Field safety notice
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