International safety notice
DEEP BRAIN ELECTRICAL STIMULATION SYSTEM
Brazil / Anvisa · BRA · May 25, 2016
Key facts
| Title | DEEP BRAIN ELECTRICAL STIMULATION SYSTEM |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial name of the product: Implantable Neurostimulator for Deep Brain Stimulation (Anvisa registration number: 10339190485), Activa RC Rechargeable Programmable Neurostimulator (Anvisa registration number: 10339190528), Activa® SC Programmable Neurostimulator (Anvisa registration number: 10339190338), DBS Extension Kit for Deep Brain Stimulation (Anvisa registration number: 10339190463); |
| Manufacturer | DETENTOR DO REGISTRO MEDTRONIC COMERCIAL LTDA CNPJ 01772798000152 ENDEREÇO AV JORNALISTA ROBERTO MARINHO 85 10º ANDAR CEP 04675010 SÃO PAULO SP TELEFONE 11 21829200 FABRICANTES1 MEDTRONIC INC ENDEREÇO 710 MEDTRONIC PARKWAY MINNEAPOLIS MN 55432 2 MEDTRONIC NEUROMODULATION ENDEREÇO 800 53RD AVENUE NE MINNEAPOLIS MN 55421ESTADOS UNIDOS 3 MEDTRONIC PUERTO RICO OPERATIONS CO MEDREL JUNCOS ENDEREÇO ENDEREÇO ROAD31 KM 24 HM 4 PR 007777 JUNCOS PORTO RICO 4 MEDTRONIC PUERTO RICO OPERATIONS CO MPRI ENDEREÇO ROAD149 KM 563 00766 VILLALBA PORTO RICO |
| Models | 10339190338, 10339190463, 10339190191, 10339190152, 10339190528, 10339190485 |
| Date | May 25, 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