International safety notice
Technical name: Anesthesia Device
Brazil / Anvisa · BRA · Dec 15, 2017
Key facts
| Title | Technical name: Anesthesia Device |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Nome comercial: (Fabius, Fabius GS, Fabius Tiro) ; Fabius GS Premium; Technical name: Anesthesia Device ANVISA registration number: 10407370 Risk class: III Affected model: 10407370026; Affected serial numbers: See Distribution List |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO DRÄGER INDÚSTRIA E COMÉRCIO LTDA CNPJ 02535707000128 ALAMEDA PUCURUÍ 51 TAMBORÉ BARUERI SP FABRICANTE DRÄGERWERK AG CO KGAA MOISLINGER ALLEE 5355 23542 LÜBECK ALEMANHA TELEFONE 4518825101 EMAIL MICHAELPETRICHDRAEGERCOM |
| Models | 10407370110, 10407370, 10407370065, 10407370026, 10407370124, 10407370061 |
| Date | Dec 15, 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