International safety notice
SX-ELLA Stent Danis Procedure Pack
Ireland / HPRA · IRL · Apr 4, 2017
Key facts
| Title | SX-ELLA Stent Danis Procedure Pack |
|---|---|
| Regulator | Ireland / HPRA |
| Country | IRL |
| Brand | SX-ELLA Stent Danis Procedure Pack |
| Manufacturer | Ella-CS |
| Models | FSN-ELLA-2017-001, 50006, TFEBE5, C.V.7507785, 019-08S-25-135, 019-08S-25-135-B |
| Event type | Safety Notice |
| Date | Apr 4, 2017 |
| Regulator page | hpra.ie |
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