International safety notice
Technical name: Leukocyte Removal Filter (Laboratory)
Brazil / Anvisa · BRA · Jun 23, 2017
Key facts
| Title | Technical name: Leukocyte Removal Filter (Laboratory) |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade name: Filter for removing leukocytes from platelet concentrates for bench use Technical name: Filter for Leukocyte Removal (Laboratory) ANVISA registration number: 10154450112 Risk class: III Affected model: COMPOSTOP Affected serial numbers: 71KE05GA00, 71KE10GA00 , 71KE25GC00 and 71KG07GA00 |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO FRESENIUS HEMOCARE BRASIL LTDA RUA ROQUE GONZALES 128 SP 11 25041481 FABRICANTE FRESENIUS HEMOCARE BRASIL LTDA RUA ROQUE GONZALES 128 SP 11 25041481 |
| Models | 10154450112, 71KE05GA00, 71KE25GC00, 71KE10GA00, 71KG07GA00 |
| Date | Jun 23, 2017 |
| 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