International safety notice
TRUMPF Medizin
United Kingdom / MHRA · GBR · Dec 21, 2015
Key facts
| Title | TRUMPF Medizin |
|---|---|
| Regulator | United Kingdom / MHRA |
| Country | GBR |
| Brand | TruLight 3000, TruLight 5000, iLED, Helion, Xenion |
| Manufacturer | TRUMPF Medizin |
| Models | 1532466, 4038210, 4028110, 1574759, 1565161, 4038110, 4038310, 1574851, 1565160, 1565068, 4028210, 4028310 and 1 more |
| Event type | Safety Notice |
| Action type | Field safety notice |
| Date | Dec 21, 2015 |
| 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