International safety notice
Technical name: ENDOTRACHEAL CANNULA/ELECTRODE
Brazil / Anvisa · BRA · Feb 10, 2017
Key facts
| Title | Technical name: ENDOTRACHEAL CANNULA/ELECTRODE |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial name: CANNULA KIT FOR RECURRENT STIMULATION WITH NIM RESPONSE STIMULATOR PROBE Technical name: ENDOTRACHEAL CANNULA/ELECTRODE ANVISA registration number: 10173550046 Risk class: II Affected model: M8229306K, M8229307K, M8229308K |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO RICHARDS DO BRASIL PRODUTOS CIRÚRGICOS LTDA CNPJ 48767628000143 ENDEREÇO AV DR DIB SAUAIA NETO 1492 ALPHAVILLE EMPRESARIAL MUNICÍPIO BARUERI UF SP TELEFONE DE CONTATO 11 3198 2999 FABRICANTE MEDTRONIC XOMED INC 6743 SOUTHPOINT DRIVE NORTH JACKSONVILLE FL 32216 0980 ESTADOS UNIDOS DA AMÉRICA |
| Models | 10173550046, M8229307K, M8229306K, M8229308K |
| Date | Feb 10, 2017 |
| 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