International safety notice
Vascular Endoprosthesis.
Brazil / Anvisa · BRA · Feb 27, 2014
Key facts
| Title | Vascular Endoprosthesis. |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Dominus Graft Stent Endoprosthesis, Straight and Straight models with Free Flow Anvisa Registration: 10159030093). |
| Manufacturer | BRAILE BIOMÉDICA INDÚSTRIA COMÉRCIO E REPRESENTAÇÕES |
| Models | 10159030093, 10159030096 |
| Date | Feb 27, 2014 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 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