International safety notice
Technical name: Anesthesia Device
Brazil / Anvisa · BRA · Jan 23, 2018
Key facts
| Title | Technical name: Anesthesia Device |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade name: Carestation Anesthesia System Technical name: Anesthesia Device ANVISA registration number: 80071260222 Risk class: III Affected model: All Affected serial numbers: 9100c (ANVISA Registration 80071260222) |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO GE HEALTHCARE DO BRASIL COM E SERV PARA EQUIPAMENTOS MÉDICOHOSPITALARES LTDA CNPJ 00029372000140 AV MAGALHÃES DE CASTRO Nº 4800 11º ANDAR CIDADE JARDIM SÃO PAULO SP FABRICANTE GE MEDICAL SYSTEMS CHINA CO LTD EMAIL TECNOVIGILANCIABRGECOM |
| Models | 80071260222, 9100c |
| Date | Jan 23, 2018 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
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