International safety notice
Technical name: Anesthesia Device
Brazil / Anvisa · BRA · May 11, 2017
Key facts
| Title | Technical name: Anesthesia Device |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial name: Carestation Anesthesia System Technical name: Anesthesia Apparatus ANVISA registration number: 80071260356 Risk class: III Affected model: Carestation 620, Carestation 650 and Carestation 650c Affected serial numbers: Models Carestation 620, Carestation 650 and Carestation 650c with software version Revision.01 |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO GE HEALTHCARE DO BRASIL COM E SERV PARA EQUIPAMENTOS MÉDICOHOSPITALARES LTDA CNPJ 00157774000554 END AV MAGALHÃES DE CASTRO Nº 4800 13º ANDAR CIDADE JARDIM SP BRASIL FABRICANTE DATEX OHMEDA INC PAÍS ESTADOS UNIDOS DA AMÉRICA |
| Models | 80071260356, Revisão.01 |
| Date | May 11, 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