International safety notice
Mammography Device
Brazil / Anvisa · BRA · May 7, 2015
Key facts
| Title | Mammography Device |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Graph Mammo and Graph Mammo DR Mammography Device, registrations 10216710296 and 10216710243, risk class III, serial number of affected equipment and municipalities located: PADPVG01001 - SANTA ROSA; PADPVG02001 - CERES; PADPW801001 - LAGES; PADPVG03001 - TERESINA; PADQKC01001 - GOIANIA; PADQKC02001 - EMPRESS; PADRNO02001 - SPRING; PADRWY02001 - ARAPIRACA; PADRNO01001 - AMARANTE; PADRWY01001 - CAPANEMA; PACZUO01001 - CACOAL; PAD63801001 - GOIANIA; PADED101001 - RIO VERDE; PADKZ801001 - MONTENEGRO. |
| Manufacturer | DETENTOR DO REGISTRO PHILIPS MEDICAL SYSTEMS LTDA CNPJ 58295213000178 ENDEREÇO AV PIRACEMA 1411 MÓDULOS 3 E 4 TAMBORÉ BARUERI SP FABRICANTE RUA PREFEITO ELIZEU ALVES DA SILVA 400 CIDADE LAGOA SANTA MG |
| Models | PADQKC02001, PADRWY02001, PADRWY01001, PACZUO01001, PADPXU01001, 10216710296, PADED101001, PADQKC01001, PADPVG01001, PADPVG03001, PADKZ801001, PADRNO01001 and 5 more |
| Date | May 7, 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