International safety notice
Technical name: Ultrasound Device
Brazil / Anvisa · BRA · Mar 24, 2017
Key facts
| Title | Technical name: Ultrasound Device |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade name: Vivid Ultrasound System Technical name: Ultrasound Device ANVISA registration number: 80071260361 Risk class: II Affected model: Vivid E80, Vivid E90, Vivid E95 Affected batch/serial numbers: Vivid E95, Vivid E90, Vivid E80 with software version 201, revision 54.0 and 61.0 |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO GE HEALTHCARE DO BRASIL COM E SERV PARA EQUIPAMENTOS MÉDICOHOSPITALARES LTDA ENDEREÇO AV MAGALHÃES DE CASTRO Nº 4800 13º ANDAR CIDADE JARDIM TELEFONE 11 30678436 FABRICANTE GE VINGMED ULTRASOUND AS GE HEALTHCARE DO BRASIL COM E SERV PARA EQUIPAMENTOS MÉDICOHOSPITALARES LTDA PAÍS NORUEGA BRASIL |
| Models | 80071260361 |
| Date | Mar 24, 2017 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models 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