International safety notice
Commercial Name: Fabius MRI - Anesthesia Workstation Technical Name: Anesthesia Device - Registration 10407370065 Risk Class III (High Risk)
Brazil / Anvisa · BRA · Aug 18, 2015
Key facts
| Title | Commercial Name: Fabius MRI - Anesthesia Workstation Technical Name: Anesthesia Device - Registration 10407370065 Risk Class III (High Risk) |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Fabius MRI - Anesthesia Workstation Technical Name: Anesthesia Device - Registration 10407370065 Risk Class III (High Risk)Model: Fabius MRI Affected Series in ANNEX (Distribution Map). |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO DRÄGER INDÚSTRIA E COMÉRCIO LTDA CNPJ 02535707000128 ENDEREÇO ALAMEDA PUCURUÍ 51 TAMBORÉ BARUERI SÃO PAULO TELEFONE 11 46894415 FABRICANTE DRÄGER MEDICAL GMBH MOISLINGER ALLE 5355 LÜBECK ALEMANHA |
| Models | 10407370065 |
| Date | Aug 18, 2015 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models 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