International safety notice
Technical Name: Electrodes (ENDOTRACHEAL CANNULA).
Brazil / Anvisa · BRA · Jul 1, 2016
Key facts
| Title | Technical Name: Electrodes (ENDOTRACHEAL CANNULA). |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial name: Cannula Kit for Recurrent Stimulation with Stimulating Probe//// ANVISA registration: 10339190172///Risk class: II Model(s) affected: 8229306, 8229307, 8229308 and Lot(s) / Serial No.(s) affected: attached document. |
| Manufacturer | DETENTOR DO REGISTRO DO PRODUTO NO BRASIL NOME MEDTRONIC COMERCIAL LTDA CNPJ 01772798000152 MUNICÍPIO SP UF SP TELEFONE DE CONTATO 1121829200 FABRICANTE MEDTRONIC XOMED INC 6743 SOUTHPOINT DRIVE NORTH JACKSONVILLE FL 32216 0980 ESTADOS UNIDOS DA AMÉRICA |
| Models | 8229307, 8229306, 8229308, 10339190172 |
| Date | Jul 1, 2016 |
| Regulator page | anvisa.gov.br |
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