International safety notice
Schülke Octenidol suuloputusvahend - kindla partii tagasikutsumine, võimalik mikrobioloogiline saastumus
Estonia / EMDDB · EST · Dec 1, 2018
Key facts
| Title | Schülke Octenidol suuloputusvahend - kindla partii tagasikutsumine, võimalik mikrobioloogiline saastumus |
|---|---|
| Regulator | Estonia / EMDDB |
| Country | EST |
| Brand | Schülke Octenidol suuloputusvahend |
| Manufacturer | SCHÜLKE OCTENIDOL SUULOPUTUSVAHEND |
| Models | 1510193, 1502589, 18.12.2018, 1507320, 1502724, 1507056, 1507799, 70000769, 22851, 1511550, 1504482, 1510617 and 5 more |
| Date | Dec 1, 2018 |
| 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