International safety notice
MAGNETIC RESONANCE EQUIPMENT / POSITRON EMISSION TOMOGRAPHY AND MAGNETIC RESONANCE EQUIPMENT (PET/MRI)
Brazil / Anvisa · BRA · Oct 15, 2015
Key facts
| Title | MAGNETIC RESONANCE EQUIPMENT / POSITRON EMISSION TOMOGRAPHY AND MAGNETIC RESONANCE EQUIPMENT (PET/MRI) |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | MAGNETIC RESONANCE IMAGING SYSTEM, models and registrations: DISCOVERY MR750W 3.0T, 80071260134 /// DISCOVERY MR 750 3.0T, 80071260110 /// Signa System, Signa PET/MR, 80071260348 /// SIGNA HDXT 3.0T and SIGNA HDXT 1.5 T, 80071260103 /// SIGNA EXCITE, HDX 1.5T and HDX 3.0T, 80071260081 /// MR SIGNA EXCITE 3.0T, 80071260061 ////. |
| Manufacturer | DETENTOR DO REGISTRO GE HEALTHCARE DO BRASIL COM E SERV PARA EQUIPAMENTOS MÉDICOHOSPITALARES LTDA CNPJ 00 029 372 0001 40 ENDEREÇO AV MAGALHÃES DE CASTRO Nº 4800 13º ANDAR CIDADE JARDIM SÃO PAULO FABRICANTE GE MEDICAL SYSTEMS LLC ENDEREÇO 3200 NORTH GRANDVIEW BOULEVARD WUAKESHA WISCONSIN 53188 EUA |
| Models | 80071260110, 80071260348, MR750W, 80071260061, 80071260134, 80071260081, 80071260103 |
| Date | Oct 15, 2015 |
| 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