International safety notice
Technical name: Magnetic Resonance Equipment
Brazil / Anvisa · BRA · Sep 8, 2016
Key facts
| Title | Technical name: Magnetic Resonance Equipment |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade name: Magnetic Resonance Imaging System Technical name: Magnetic Resonance Equipment ANVISA registration number: 80071260358 Risk class: II Affected model: Signa Pioneer Affected serial numbers: MAGiC (MAGnetic resonance imaging compilation) on Signa Pioneer and on systems running Application software, version DV25.1. |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO GE HEALTHCARE DO BRASIL COM E SERV PARA EQUIPAMENTOS MÉDICOHOSPITALARES LTDA ENDEREÇO AV MAGALHÃES DE CASTRO Nº 4800 13º ANDAR CIDADE JARDIM SP TELEFONE 11 30678436 FABRICANTE GE HEALTHCARE JAPAN CORPORATION PAÍS JAPÃO |
| Models | DV25.1, 80071260358 |
| Date | Sep 8, 2016 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 1–9 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