International safety notice
Physiological Fluid Analyzer
Brazil / Anvisa · BRA · Jul 24, 2017
Key facts
| Title | Physiological Fluid Analyzer |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial name: cobas e 602, cobas e 601 and E170 modules Technical name: Physiological Fluid Analyzer ANVISA registration number: 10287410597; Risk class: I and II Affected model: Affected serial numbers: 4745922001, 5990378001, 4998642001, 3617505001 |
| 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, 3617505001, 4745922001, 5990378001, 10287410671, 4998642001, 10287410878 |
| Date | Jul 24, 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