International safety notice
Technical Name: Anesthesia Device
Brazil / Anvisa · BRA · Feb 26, 2016
Key facts
| Title | Technical Name: Anesthesia Device |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | The products affected by this field action are registered with ANVISA as: (i). |
| Manufacturer | DADOS DO DETENTOR DO REGISTRO NO BRASIL GE HEALTHCARE DO BRASIL COM E SERV PARA EQUIPAMENTOS MÉDICOHOSPITALARES LTDA CNPJ 00029372000140 ENDEREÇO AV MAGALHÃES DE CASTRO Nº 4800 13º ANDAR CIDADE JARDIM SÃO PAULOSP TEL 11 30678436 NOME DA EMPRESA FABRICANTE DATEXOHMEDA INC PAÍS ESTADOS UNIDOS ENDEREÇO 3030 OHMEDA DRIVE MADISON WI |
| Models | 80071260326, 80071260272, 840682102292 |
| Date | Feb 26, 2016 |
| 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