International safety notice
X-ray device
Brazil / Anvisa · BRA · Jul 3, 2015
Key facts
| Title | X-ray device |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | X-ray device, Compact Plus, risk class III, registration 10216710251, affected series/batches attached. |
| Manufacturer | DETENTOR DO REGISTRO PHILIPS MEDICAL SYSTEMS LTDA CNPJ 58295213000178 ENDEREÇO AV PIRACEMA 1411 MÓDULOS 3 E 4 TAMBORÉ BARUERI SP FABRICANTE PHILIPS MEDICAL SYSTEMS LTDA ENDEREÇO RUA PREFEITO ELIZEU ALVES DA SILVA 400 CIDADE LAGOA SANTA MG |
| Models | 10216710251 |
| Date | Jul 3, 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