International safety notice
Technical name: Mammography Device
Brazil / Anvisa · BRA · Feb 10, 2017
Key facts
| Title | Technical name: Mammography Device |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial name: Digital Mammography Device Technical name: Mammography Device ANVISA registration number: 10345162027 Risk class: III Affected model: MAMMOMAT Inspiration Affected serial numbers: 3063; |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO SIEMENS HEALTHCARE DIAGNÓSTICOS SA CNPJ 01449930000190 ENDEREÇO AV MUTINGA 3800 7º ANDAR PIRITUBA SÃO PAULOSP TELEFONE 0800 129 633 FABRICANTE SIEMENS AG WITTELSBACHERPLATZ 2 DE80333 MUENCHEN ALEMANHA |
| Models | 10345162027 |
| Date | Feb 10, 2017 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
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