International safety notice
Technical Name: INFUSION PUMP
Brazil / Anvisa · BRA · Feb 29, 2016
Key facts
| Title | Technical Name: INFUSION PUMP |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Product affected by Field Action: SynchroMed II Implantable Infusion Pump (Registration 10339190229) Models 8637-20, 8637-40 Risk Class IV. |
| Manufacturer | DADOS DO DETENTOR DO REGISTRO NO BRASIL MEDTRONIC COMERCIAL LTDA CNPJ 01772798000152 ENDEREÇO AV JORNALISTA ROBERTO MARINHO 85 9º ANDAR PARTE E 10º ANDAR PARTE CEP 04675010 SÃO PAULOSP TEL 11 21829200 EMPRESA FABRICANTE MEDTRONIC INC ESTADOS UNIDOS DA AMÉRICA FABRICAR |
| Models | 8637-20, 10339190229, 8637-40 |
| Date | Feb 29, 2016 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models in FDA data
- 1–9 Matching catalog numbers in FDA data
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