International safety notice
Device for determining clotting time
Brazil / Anvisa · BRA · Jul 10, 2017
Key facts
| Title | Device for determining clotting time |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial name: CA SERIE 500/600 AUTOMATIC COAGULATION ANALYZER SYSMEX Technical name: Device for Determination of Coagulation Time ANVISA registration number: 10345161731 Risk class: I Affected model: Sysmex CA-620; |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO SIEMENS HEALTHCARE DIAGNÓSTICOS SA CNPJ 01449930000190 ENDEREÇOAV MUTINGA 3800 4º ANDAR PIRITUBA SÃO PAULO SP TELEFONE 0800129 633 FABRICANTE SYSMEX CORPORATION 3142 KITANO NOGUCHICHO KAKOGAWA HYOGO 6750011 JAPÃO |
| Models | 12187, 12188, 13072, 12715, 13127, 13125, 12760, 13073, 12711, 12634, 13071, 11753 and 38 more |
| Date | Jul 10, 2017 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 100–999 Matching device models in FDA data
- 100–999 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