International safety notice
Technical Name: Infusion Pump
Brazil / Anvisa · BRA · Nov 17, 2017
Key facts
| Title | Technical Name: Infusion Pump |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade name: Synchromed II Implantable Infusion Pump Technical Name: Infusion Pump ANVISA registration number: 10339190229 Risk class: IV Affected model: 8637-20 AND 8637-40 Affected serial numbers: See list of Distribution and Affected Lots |
| 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 | 8637-40, 10339190229, 8637-20 |
| Date | Nov 17, 2017 |
| 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