International safety notice
Angiography Equipment
Brazil / Anvisa · BRA · Jul 24, 2015
Key facts
| Title | Angiography Equipment |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Angiography equipment, risk class III: AXIOM ARTIS FC, registration 10234230075, batches/series: 10151, 10279, 10312, 10320, 10379, 10409, 10481, 10501, 10513, 10520, 10526, 10 533./// AXIOM ARTIS FA , registration: 10234230093, lots/series: 25062; |
| Manufacturer | DETENTORA DO REGISTRO NO BRASIL SIEMENS LTDA CNPJ 44013159000116 ENDEREÇO AV MUTINGA 3800 7º ANDAR PIRITUBA SÃO PAULO SP FABRICANTE SIEMENS AG ENDEREÇO WITTELSBACHERPLATZ 2 DE80333 MUENCHEN ALEMANHA |
| Models | 10481, 137045, 136276, 25418, 147551, 135941, 35748, 35862, 137088, 25330, 137182, 160360 and 134 more |
| Date | Jul 24, 2015 |
| 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