International safety notice
Welch Allyn patsiendikaablite ja juhtmete komplektid - TÄIENDATUD tagasikutsumine, ei vasta nõuetele
Estonia / EMDDB · EST · Jul 1, 2020
Key facts
| Title | Welch Allyn patsiendikaablite ja juhtmete komplektid - TÄIENDATUD tagasikutsumine, ei vasta nõuetele |
|---|---|
| Regulator | Estonia / EMDDB |
| Country | EST |
| Brand | Welch Allyn patsiendikaablite ja juhtmete komplektid |
| Manufacturer | WELCH ALLYN PATSIENDIKAABLITE JA JUHTMETE KOMPLEKTID |
| Models | 9293-033-53, 17788, 9293-046-61, 9293-017-50, 60601-2-25, E2-E4, 9293-047-65, 9293-047-60, 10WIRE, 9293-026-51, 9293-028-51, 67790 and 35 more |
| 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