International safety notice
Technical name: Mobile X-ray Device
Brazil / Anvisa · BRA · Oct 4, 2016
Key facts
| Title | Technical name: Mobile X-ray Device |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial name: Radiographic Mobile C-Arm Technical name: Mobile X-ray Device ANVISA registration number: 80071260301 Risk class: III Affected model: Brivo OEC 715, Brivo OEC 785, Brivo OEC 865 Affected serial numbers: GE Brivo OEC715: Serial Numbers B2S15158 to B2S15164; |
| 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 HUALUN MEDICAL SYSTEMS CO LTD GE HEALTHCARE DO BRASIL COM E SERV PARA EQUIPAMENTOS MÉDICOHOSPITALARES LTDA PAÍS CHINA BRASIL |
| Models | B2S15158, B4S15063, B2S15173, B2S15171, B4S15075, B3S15253, B2S15197, B3S15359, B3S15353, B4S15073, B4S15070, B2S15195 and 24 more |
| Date | Oct 4, 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