International safety notice
Mammography Device
Brazil / Anvisa · BRA · Mar 5, 2015
Key facts
| Title | Mammography Device |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Graph-Mammo AF Mammography Device, registration: 10216710241, risk class III, Philips brand; |
| Manufacturer | DETENTOR DO REGISTRO PHILIPS MEDICAL SYSTEMS LTDA CNPJ AV PIRACEMA 1411 MÓDULOS 3 E 4 TAMBORÉ BARUERI SÃO PAULO FABRICANTE PHILIPS MEDICAL SYSTEMS ENDEREÇO RUA PREFEITO ELIZEU ALVES DA SILVA 400 CEP 33400000 LAGOA SANTA MINAS GERAIS BRASIL |
| Models | PABI8101001, 10216710241, PACHD401001 |
| Date | Mar 5, 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