International safety notice
Angiography System
Brazil / Anvisa · BRA · Jul 2, 2015
Key facts
| Title | Angiography System |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Angix Digital Angiography System, registration 80260940003, risk class III. |
| Manufacturer | DETENTOR DO REGISTRO E FABRICANTE XPRO SISTEMAS LTDA CNPJ 02173632000182 ENDEREÇO AV CRISITANO MACHADO 1989 SILVEIRA CEP 31140535BELO HORIZONTE MG |
| Models | 80260940003 |
| Date | Jul 2, 2015 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models in FDA data
- 1–9 Matching catalog numbers in FDA data
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