International safety notice
CEPA GLICOCHEK Registration: 80047580143 Risk Class II Medium Risk
Brazil / Anvisa · BRA · Nov 6, 2014
Key facts
| Title | CEPA GLICOCHEK Registration: 80047580143 Risk Class II Medium Risk |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | CEPA GLICOCHEK Registration: 80047580143 Risk Class II Medium Risk - Technical name: Glucose Meter Model: CEPA GLICOCHEK TD-4230 (AFFECTED SERIES Annex)(DISTRIBUTION MAP - Annex). |
| Manufacturer | DETENTOR DO REGISTRO NO BRASIL MBIOLOG DIAGNOSTICOS LTDA CNPJ 03590360000189 RUA GAMMA 337 VILA PARIS CONTAGEMMG FAX 31 35070707 FABRICANTE TAIDOC TECHNOLOGY CORPORATION TAIWAN |
| Models | 80047580143, TD-4230 |
| Date | Nov 6, 2014 |
| 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