International safety notice
URIC ACID
Brazil / Anvisa · BRA · Jul 30, 2015
Key facts
| Title | URIC ACID |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Reflotron Uric Acid, Registration: 10287410183, Lots: 20750002, 21149403, 21836402, 21625703, 21506202, 22222403, 22311502, 22500902, 22618503, 2291 5302, 23179404, 23336508 |
| Manufacturer | DETENTOR DO REGISTRO NO BRASIL ROCHE DIAGNÓSTICA BRASIL LTDA CNPJ 30280358000186 ENDEREÇO AVENIDA ENGENHEIRO BILLINGS 1729 PRÉDIO 38 SÃO PAULO SÃO PAULO FABRICANTE ROCHE DIAGNOSTICS GMBH ALEMANHA |
| Models | 21506202, 22618503, 21625703, 10287410183, 22311502, 20750002, 22500902, 21149403, 23336508, 21836402, 22915302, 22222403 and 1 more |
| Date | Jul 30, 2015 |
| 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