International safety notice
Fixed X-ray Device
Brazil / Anvisa · BRA · Dec 16, 2014
Key facts
| Title | Fixed X-ray Device |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | PROTEUS X/Ra X-ray System, Risk class III, Model 600-0301, Registration: 80071260005, manufactured before January 2011. Serial numbers: 00000024890HL6; |
| 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 HUALUN MEDICAL SYSTEMS CO LTDA ENDEREÇO NO 1 YONG CHANG NORTH ROAD ECONOMIC TECHNOLOGICAL DEVELOPMENT ZONE BEIJING PR CHINA 100176 |
| Models | 80071260005, 00000024770HL0, 00000025100HL9, 00000025102HL5, 00000024890HL6, 600-0301, 00000024891HL4, FMITR170990633, 00000022726HL4, 00000024837HL7, 00000025105HL8 |
| Date | Dec 16, 2014 |
| 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