International safety notice
Vaporizer
Brazil / Anvisa · BRA · Jun 28, 2016
Key facts
| Title | Vaporizer |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial name of the product: ANESTHETIC VAPORIZERS /// Registration number: 10407370119/// Affected model(s): D-Vapor/// Product risk class: III. |
| Manufacturer | DETENTOR DO REGISTRO DRAGER INDUSTRIA E COMERCIO LTDA CNPJ 02535707000128 ENDEREÇO ALAMEDA PUCURUI 51 BARUERI SP 11 46894415 FABRICANTES DRAGERWERK AG CO KGAA ENDEREÇO MOISLINGER ALLE 5355 LUBECK ALEMANHA |
| Models | 10407370119 |
| Date | Jun 28, 2016 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 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