International safety notice
Allergan XEN Glaucoma Treatment System - tagasikutsumine, tootmisprotsessis kasutatava poleerija jäägid seadmes
Estonia / EMDDB · EST · Nov 1, 2019
Key facts
| Title | Allergan XEN Glaucoma Treatment System - tagasikutsumine, tootmisprotsessis kasutatava poleerija jäägid seadmes |
|---|---|
| Regulator | Estonia / EMDDB |
| Country | EST |
| Brand | Allergan XEN Glaucoma Treatment System |
| Manufacturer | ALLERGAN XEN GLAUCOMA TREATMENT SYSTEM |
| Models | 62263, 61685, 61846, 61626, FSN-19-001, 62130, 62297, 0035316445224, 61642, 62008, 61580, 61566 and 17 more |
| Date | Nov 1, 2019 |
| Regulator page | terviseamet.ee |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models in FDA data
- 1–9 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