International safety notice
Magnetic Resonance Equipment
Brazil / Anvisa · BRA · Jan 26, 2015
Key facts
| Title | Magnetic Resonance Equipment |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Magnetic Resonance Imaging System, Model: DISCOVERY MR450 - Registration 80071260116 Serial Numbers: This correction applies to all GE Healthcare Magnetic Resonance Imaging (MRI) systems with superconducting magnets. |
| Manufacturer | DETENTOR DO REGISTRO NO BRASIL GE HEALTHCARE DO BRASIL COM E SERV PARA EQUIPAMENTOS MÉDICOSHOSPITALARES LTDA CNPJ 68867522000129 ENDEREÇO AV MAGALHÃES DE CASTRO Nº4800 13º ANDAR CIDADE JARDIM SÃO PAULO SP FABRICANTE GE MEDICAL SYSTEMS LLC 3200 N GRANDVIEW BLVD WAUKESHA WI 53188 ESTADOS UNIDOS |
| Models | 80071260116, MR450 |
| Date | Jan 26, 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