International safety notice
Diagnostic Ultrasound System
Brazil / Anvisa · BRA · Jul 24, 2015
Key facts
| Title | Diagnostic Ultrasound System |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | ACUSON diagnostic ultrasound system, ACUSON S1000 models; |
| Manufacturer | DETENTORA DO REGISTRO NO BRASIL SIEMENS LTDA CNPJ 44013159000116 ENDEREÇO AV MUTINGA 3800 7º ANDAR PIRITUBA SÃO PAULO SP FABRICANTE SIEMENS MEDICAL SOLUTIONS USA INC E SIEMENS LTDA ENDEREÇOS 685 EAST MIDDLEFIELD ROAD MONTAIN VIEW CALIFORNIA 94043 E RUA DONA FRANCISCA 8300 BLOCO K MÓDULO 1 JOINVILLE |
| Models | VC31A, S2000, 210786, S1000, VC30A, 211080, 202134, VC30C, 211085, 10234230192, VC30B, 211397 |
| Date | Jul 24, 2015 |
| 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