International safety notice
Magnetic Resonance Equipment
Brazil / Anvisa · BRA · Feb 25, 2016
Key facts
| Title | Magnetic Resonance Equipment |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Discovery MR 750 3.0T model Discovery MR 750 3.0T, registration 80071260110 and Imaging and Magnetic Resonance System, model Discovery MR 750w 3.0T, registration 80071260134, risk class II, batch/series 0000040-4-0161; |
| Manufacturer | DETENTOR DO REGISTRO GE HEALTHCARE DO BRASIL COM E SERV PARA EQUIPAMENTOS MÉDICOHOSPITALARES LTDA ENDEREÇO AV MAGALHÃES DE CASTRO Nº 4800 13º ANDAR CIDADE JARDIM SÃO PAULOSP FABRICANTE NOME DA EMPRESA FABRICANTE GE MEDICAL SYSTEMS LLC PAÍS ESTADOS UNIDOS ENDEREÇO 3000 N GRANDVIEW BLVD WAUKESHA WI 53188 |
| Models | 0000033-4-0161, 000032E-4-0160, 000032E-4-0313, 000032E-4-0181, 0000033-4-0145, 80071260134, 0000004-4-0242, 0000034-4-0242, 0000034-4-0152, 0000040-4-0258, 0000033-4-0261, 0000033-4-0443 and 6 more |
| Date | Feb 25, 2016 |
| 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