International safety notice
Technical name: High Frequency Surgical Equipment/Electrode
Brazil / Anvisa · BRA · Jul 12, 2016
Key facts
| Title | Technical name: High Frequency Surgical Equipment/Electrode |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial name: Valleylab Force Argon II System/Electrode for Laparoscopy Valleylab Technical name: High Frequency Surgical Equipment/Electrode ANVISA registration number: 10349000185/10349000216 |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO AUTO SUTURE DO BRASIL LTDA CNPJ 01645409000128 ENDEREÇO AV JORNALISTA ROBERTO MARINHO 85 10º ANDAR 04675010 MUNICÍPIO SÃO PAULO UF |
| Models | 10349000216, 10349000185 |
| Date | Jul 12, 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