International safety notice
Alert 2789 (Technosurveillance) - Medtronic - Implantable Pacemaker With MRI Surescan Technology - Dual Chamber;
Brazil / Anvisa · BRA · Jan 28, 2019
Key facts
| Title | Alert 2789 (Technosurveillance) - Medtronic - Implantable Pacemaker With MRI Surescan Technology - Dual Chamber; |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade Name: Implantable Pacemaker With MRI Surescan Technology Dual Chamber (registration no. 10339190710); |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO MEDTRONIC COMERCIAL LTDA CNPJ 01772798000152 AV JORNALISTA ROBERTO MARINHO 85 10º ANDAR CEP 04675010 SÃO PAULO SP TEL 11 21829200 EMAIL TECNOVIGILANCIACOVIDIENCOM FABIOLACAPPELLARIMEDTRONICCOM FABRICANTE DO PRODUTO MEDTRONIC SINGAPORE OPERATIONS PTE LTD 49 CHANGI SOUTH AVENUE 2 NOSACO TECH CENTRE 486056 SINGAPORE |
| Models | ADDRS1, ATDRS1, 10339190277, ATDR01, 10339190710, ATDRL1 |
| Date | Jan 28, 2019 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models 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