International safety notice
Technical name: CABLE/ELECTRODE FOR DEEP BRAIN ELECTRICAL STIMULATION SYSTEM
Brazil / Anvisa · BRA · Nov 16, 2017
Key facts
| Title | Technical name: CABLE/ELECTRODE FOR DEEP BRAIN ELECTRICAL STIMULATION SYSTEM |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade name: DBS Electrode for Deep Brain Stimulation Technical name: CABLE/ELECTRODE FOR DEEP BRAIN ELECTRICAL STIMULATION SYSTEM ANVISA registration number: 10339190484 Risk class: IV Affected model: 3387/3387-28/3387-40/3387S/3387-40 Affected serial numbers: see attachment |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO MEDTRONIC COMERCIAL LTDA CNPJ 01772798000152 AV JORNALISTA ROBERTO MARINHO 85 10º ANDAR CEP 04675010 SÃO PAULO SP FABRICANTE MEDTRONIC INC 710 MEDTRONIC PARKWAY MINNEAPOLIS MN 55432 ESTADOS UNIDOS |
| Models | 10339190484, 3387S, 3387-28, 3387-40 |
| Date | Nov 16, 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