International safety notice
Hemodialysis Device
Brazil / Anvisa · BRA · Feb 15, 2016
Key facts
| Title | Hemodialysis Device |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Hemodialysis machine, Dialog + and Dialog + HDF online models (7102005, 7102072, 710200C and 710207E), registration 80136990498, risk class III, various series (SEE ANNEX). |
| Manufacturer | DETENTOR DO REGISTRO LABORATÓRIOS B BRAUN SA ENDEREÇO AV EUGÊNIO BORGES 1092 E AV JEQUITIBÁ 9 SÃO GONÇALORJ CEP 24751000 FABRICANTE B BRAUN AVITUM AG ENDEREÇO SCHWARZENBERGER WEG 7379 MELSUNGENALEMANHA |
| Models | 710200C, 7102005, 7102072, 710207E, 80136990498 |
| Date | Feb 15, 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