International safety notice
Angiography Equipment.
Brazil / Anvisa · BRA · Nov 16, 2012
Key facts
| Title | Angiography Equipment. |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | ARTIS ANGIOGRAPHY EQUIPMENT. |
| Manufacturer | DETENTOR DE REGISTRO SIEMENS LTDA CNPJ 44013159000116 END AV MUTINGA 3800 PIRITUBA SÃO PAULO |
| Models | 135758, 136320, 136301, 10501, 10234230158, 136199, 136282, 135825, 35817, 35748, 160360, 136373 and 17 more |
| Date | Nov 16, 2012 |
| 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