International safety notice
Technical name: Ultrasound Device
Brazil / Anvisa · BRA · Apr 27, 2017
Key facts
| Title | Technical name: Ultrasound Device |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial name: ACUSON Diagnostic Ultrasound System Technical name: Ultrasound Device ANVISA registration number: 10345162017 Risk class: II Affected model: ACUSON S2000 Affected serial numbers: 211771; |
| 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 MEDICAL SOLUTIONS USA INC 685 EAST MIDDLEFIELD ROAD MOUNTAIN VIEW CA 94043 ESTADOS UNIDOS DA AMÉRICA |
| Models | 10345162017, 213886, 211771, 213087, 213936, 213596, 211784, S2000, 214179, 214493 |
| Date | Apr 27, 2017 |
| 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