International safety notice
Commercial name: ULTRASONIC DOPPLER SYSTEM ACUSON SEQUOIA # Registration with Anvisa: 10234230133 # Risk Class: II (Medium risk) # Technical Name: "Doppler" Ultrasonic System
Brazil / Anvisa · BRA · Sep 15, 2014
Key facts
| Title | Commercial name: ULTRASONIC DOPPLER SYSTEM ACUSON SEQUOIA # Registration with Anvisa: 10234230133 # Risk Class: II (Medium risk) # Technical Name: "Doppler" Ultrasonic System |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial name: ACUSON SEQUOIA ULTRASONIC DOPPLER SYSTEM # Registration with Anvisa: 10234230133 # Risk Class: II (Medium risk) # Technical Name: "Doppler" Ultrasonic System # Model: Acuson Sequoia C512/C256/512 # Affected series : 40507963, 41008034, 41008038, 41608093 |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO NO BRASIL SIEMENS LTDA CNPJ 44013159000116 ENDEREÇO AV MUTINGA 3800 PIRITUBA SÃO PAULOSP TELEFONE 11 39083876 FABRICANTE SIEMENS MEDICAL SOLUTIONS USA INC 1230 SHOREBIRD WAY MOUNTAIN VIEW CALIFÓRNIA 94043 ESTADOS UNIDOS |
| Models | 41008034, 40507963, 41008038, 10234230133, 41608093 |
| Date | Sep 15, 2014 |
| 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