International safety notice
Angiography Equipment
Brazil / Anvisa · BRA · Jun 7, 2015
Key facts
| Title | Angiography Equipment |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Angiography Equipment, Image Guided System, Model INNOVA IGS 530, Risk class III, Registration: 80071260269, serial number of the affected unit: XV650620BU8. |
| Manufacturer | DETENTOR DO REGISTRO GE HEALTHCARE DO BRASIL CNPJ 00 029 372 0001 40 ENDEREÇO AV MAGALHÃES DE CASTRO Nº 4800 13º ANDAR CIDADE JARDIM SÃO PAULO FABRICANTE GE MEDICAL SYSTEM SCS ENDEREÇO RUA DE LA MINIERE 283 BUCFRANÇA |
| Models | XV650620BU8, 80071260269 |
| Date | Jun 7, 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