International safety notice
Technical name: Device for Determining Coagulation Parameters
Brazil / Anvisa · BRA · Feb 10, 2017
Key facts
| Title | Technical name: Device for Determining Coagulation Parameters |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial name: AUTOMATIC BLOOD COAGULATION ANALYSIS SYSTEM Technical name: Apparatus P/Deter.dos Parametros de Coagulacao ANVISA registration number: 0345161778; |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO SIEMENS HEALTHCARE DIAGNÓSTICOS SA CNPJ 01449930000190 ENDEREÇO AV MUTINGA 3800 7º ANDAR PIRITUBA SÃO PAULOSP TELEFONE 0800 129 633 FABRICANTE SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH EMILVONBEHRINGSTRASSE 76 35041 MARBURG ALEMANHA |
| Models | 10345161920, 0345161778, CS-5100, CS-2100i |
| Date | Feb 10, 2017 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
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