International safety notice
Angiography Equipment.
Brazil / Anvisa · BRA · Nov 18, 2015
Key facts
| Title | Angiography Equipment. |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Equipamento para Angiografia Allura Xper. Modelo(s): FD10 (chão); FD10 (teto); FD20 (chão); FD20 (teto); FD10 OR Table; FD20 OR Table; FD10/10; FD20/20; FD20/10; FD10/10 OR Table; FD20/20 OR Table; FD20/10 OR Table. Registro Anvisa n° 10216710153. |
| Manufacturer | DETENTOR DE REGISTRO PHILIPS MEDICAL SYSTEMS LTDACNPJ 58295213000178 FABRICANTE PHILIPS MEDICAL SYSTEMS NEDERLAND BV HOLANDA |
| Models | 10216710153 |
| Date | Nov 18, 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