International safety notice
Technical name: D-DIMER
Brazil / Anvisa · BRA · Nov 25, 2016
Key facts
| Title | Technical name: D-DIMER |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial name: D-Dimer Turbo IMMULITE/IMMULITE 1000 Technical name: D-DIMER ANVISA registration number: 10345161779 Risk class: III Affected model: kit for 100 tests Affected serial numbers: 346 |
| 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 LTD GLYN RHONWN LLANBERIS CAERNARFON GWYNEDD LL55 4EL REINO UNIDO |
| Models | 10345161779 |
| Date | Nov 25, 2016 |
| 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