International safety notice
Surgical Arc
Brazil / Anvisa · BRA · Jul 28, 2017
Key facts
| Title | Surgical Arc |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade name: CIOS ALPHA Surgical Arc Technical name: Surgical Arc ANVISA registration number: 10345162008 Risk class: III Affected model: CIOS ALPHA Affected serial numbers: 12021 |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO SIEMENS HEALTHCARE DIAGNÓSTICOS SA CNPJ 01449930000190 AV MUTINGA 3800 7º ANDAR PIRITUBA SÃO PAULO SP FABRICANTE SIEMENS AG SIEMENS HEALTHCARE GMBH 1385 WITTELSBACHERPLATZ 2 DE80333 MUENCHEN HENKESTRASSE 127 DE91052 ERLANGEN ALEMANHA |
| Models | 12021, 10345162008 |
| Date | Jul 28, 2017 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 100–999 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