International safety notice
DIALYSERS
Brazil / Anvisa · BRA · Apr 11, 2013
Key facts
| Title | DIALYSERS |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | DIACAP ULTRA - FILTER FOR DIALYSIS FLUID - Registration 8013990617 - Lots/Series affected - See attachment. |
| Manufacturer | DETENTOR DO REGISTRO NO BRASIL LABORATÓRIOS B BRAUN SA SÃO GONÇALORJ |
| Models | 8013990617, 548ea4004f3917f0b097f8d785749fbd |
| Date | Apr 11, 2013 |
| 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