International safety notice
Teleflex Medical
United Kingdom / MHRA · GBR · Oct 28, 2016
Key facts
| Title | Teleflex Medical |
|---|---|
| Regulator | United Kingdom / MHRA |
| Country | GBR |
| Brand | Mucosal Atomization Device (MAD) |
| Manufacturer | Teleflex Medical |
| Event type | Safety Notice |
| Action type | Field safety notice |
| Date | Oct 28, 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