International safety notice
Technical name: Hemostasis Analyzer
Brazil / Anvisa · BRA · Jan 13, 2017
Key facts
| Title | Technical name: Hemostasis Analyzer |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial name: Multiplate® Analyzer Technical name: Hemostasis Analyzer ANVISA registration number: 10287411001 Risk class: I Affected model: Affected serial numbers: List of serial numbers distributed in Brazil and potentially affected: 100120; |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO ROCHE DIAGNÓSTICA BRASIL LTDACNPJ 30280358000186 AVENIDA ENGENHEIRO BILLINGS 1729 PRÉDIO 38 SÃO PAULO SP TEL 08007720295 FABRICANTE ROCHE DIAGNOSTICS GMBH SANDHOFER STRASSE 116 68305 ALEMANHA |
| Models | 10287411001, 101527, 101430, 101340, 101438, 100933, 100120, 101612, 101342, 101567, 101328, 100296 and 1 more |
| Date | Jan 13, 2017 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models 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