International safety notice
Teleflex laseroperatsioonides kasutatavad toru, trahheotoomiavoolik, endotrahheaaltoru - laserkiire kaitsefooliumi eraldumine
Estonia / EMDDB · EST · Apr 1, 2019
Key facts
| Title | Teleflex laseroperatsioonides kasutatavad toru, trahheotoomiavoolik, endotrahheaaltoru - laserkiire kaitsefooliumi eraldumine |
|---|---|
| Regulator | Estonia / EMDDB |
| Country | EST |
| Brand | Teleflex laseroperatsioonides kasutatavad toru, trahheotoomiavoolik, endotrahheaaltoru |
| Manufacturer | TELEFLEX LASEROPERATSIOONIDES KASUTATAVAD TORU TRAHHEOTOOMIAVOOLIK ENDOTRAHHEAALTORU |
| Models | 17511, 17361, 14151, 15391, 17241, 14261, 16191, 14441, 18121, 16081, 14491, 16431 and 178 more |
| Date | Apr 1, 2019 |
| Regulator page | terviseamet.ee |
At a glance
- No Recall
- No Field safety notice
- 100–999 Matching device models in FDA data
- 100–999 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