International safety notice
Ultrasound device
Brazil / Anvisa · BRA · Feb 3, 2016
Key facts
| Title | Ultrasound device |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | ULTRA-SOM DIAGNOSTIC SYSTEM, model ACUSON SC2000 registration 10345161999 - Risk class II. |
| Manufacturer | DETENTOR DO REGISTRO SIEMENS HEALTHCARE DIAGNÓSTICOS SA ENDEREÇO AV MUTINGA 3800 7º ANDARPIRITUBASP FABRICANTE SIEMENS MEDICAL SOLUTIONS USA INC ENDEREÇO 685 EAST MIDDLEFIELD ROAD MONTAIN VIEW CALIFORNIA 94043 ESTADOS UNIDOS |
| Models | 400831, 401809, 400762, 400723, 10345161999, 400758, SC2000 |
| Date | Feb 3, 2016 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 1–9 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