International safety notice
Magnetic Resonance Equipment
Brazil / Anvisa · BRA · Jul 20, 2015
Key facts
| Title | Magnetic Resonance Equipment |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Magnetic Resonance Equipment, risk class II: MR SIGNA EXCITE, models 1.5T and 3T, registration 80071260061 /// Signa Excite, model Signa HD 1.5T and Signa HD3.0T, registration 80071260088 /// Signa Excite, model HDx1. 5T and HDx3.0T, registration 80071260081 /// Magnetic Resonance, Signa HDxt 1.5T and Signa HDxt 3.0T, registration 80071260103 /// Signa Hdi, registration 80071260102. |
| Manufacturer | DETENTOR DO REGISTRO GE HEALTHCARE DO BRASIL CNPJ 00 029 372 0001 40 ENDEREÇO AV MAGALHÃES DE CASTRO Nº 4800 13º ANDAR CIDADE JARDIM SÃO PAULO FABRICANTE GE MEDICAL SYSTEMS LLC 3000 GRANDVIEW BLDV WAUKESHA WI 53188 ESTADOS UNIDOS |
| Models | 80071260103, 80071260081, HDx1.5T, HDx3.0T, 80071260102, 80071260088, 80071260061, HD3.0T |
| Date | Jul 20, 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