International safety notice
Glucose Meter
Brazil / Anvisa · BRA · Jan 22, 2015
Key facts
| Title | Glucose Meter |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Glucose measurements, Accu-Chek Inform II Base Unit and Handheld Base Unit, registration 10287410863, risk class II, affected batches: 05802151 to 05205301 and 05809021 to 05205311. |
| 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 SANDHOFER STRASSE 116 68305 ALEMANHA |
| Models | 10287410863, 05809021, 05205301, 05802151, 05205311 |
| Date | Jan 22, 2015 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 10–99 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