International safety notice
Karl Storz T-Lueriga ühekanalilised painduvad endoskoobid - CIDEX OPA kui käsitsi desinfitseerimise meetodi eemaldamine kasutusjuhendist
Estonia / EMDDB · EST · Apr 1, 2022
Key facts
| Title | Karl Storz T-Lueriga ühekanalilised painduvad endoskoobid - CIDEX OPA kui käsitsi desinfitseerimise meetodi eemaldamine kasutusjuhendist |
|---|---|
| Regulator | Estonia / EMDDB |
| Country | EST |
| Brand | Karl Storz T-Lueriga ühekanalilised painduvad endoskoobid |
| Manufacturer | KARL STORZ TLUERIGA ÜHEKANALILISED PAINDUVAD ENDOSKOOBID |
| Models | 11278AIK1, 11278AK1, 11292DEK1, 11278AUK1, 11272VUK, 11274AA1, 11278AIUK1, 96216006, 11005BCK1, 11292AD1, 11274AAUK1, 11278A1 and 39 more |
| Date | Apr 1, 2022 |
| Regulator page | terviseamet.ee |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models 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