International safety notice
DMD Groupe Anios Quitanet Ultra - tagasikutsumine, tooraine võimalik mikrobioloogiline saastatus
Estonia / EMDDB · EST · Jul 1, 2020
Key facts
| Title | DMD Groupe Anios Quitanet Ultra - tagasikutsumine, tooraine võimalik mikrobioloogiline saastatus |
|---|---|
| Regulator | Estonia / EMDDB |
| Country | EST |
| Brand | DMD Groupe Anios Quitanet Ultra |
| Manufacturer | DMD GROUPE ANIOS QUITANET ULTRA |
| Models | C02414S, 2762092L6, 59260, l’Espoir59260 |
| Date | Jul 1, 2020 |
| Regulator page | terviseamet.ee |
At a glance
- No Recall
- No 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