International safety notice
Physiological Fluid Analyzer: cobas c 501 module and cobas c 502 module
Brazil / Anvisa · BRA · Aug 10, 2017
Key facts
| Title | Physiological Fluid Analyzer: cobas c 501 module and cobas c 502 module |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial name: Cobas c 501 module and cobas c 502 module Technical name: Physiological Fluid Analyzer ANVISA registration number: 10287410597 and 10287410878 Risk class: I and II Affected model: Affected serial numbers: 4745914001, 5964067001 |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO ROCHE DIAGNÓSTICA BRASIL LTDA CNPJ 30280358000186 AVENIDA ENGENHEIRO BILLINGS 1729 PRÉDIO 38 SÃO PAULO SP FABRICANTE ROCHE DIAGNOSTICS GMBH 1 SANDHOFER STRASSE 116 68305 ALEMANHA EMAIL BRASILTECNOVIGILANCIAROCHECOM |
| Models | 10287410597, 4745914001, 10287410878, 5964067001 |
| Date | Aug 10, 2017 |
| 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