International safety notice
Diagnostic kit
Brazil / Anvisa · BRA · Mar 13, 2015
Key facts
| Title | Diagnostic kit |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | IMMULITE 2000/ 2000 XPi GI-MA diagnostic kit (CA 19-9), Risk class III, Registration: 10345160776, Lots 312 and 313. All products are in stock. |
| Manufacturer | DETENTOR DO REGISTRO SIEMENS HEALTHCARE DIAGNÓSTICOS LTDA CNPJ 01449930000190 ENDEREÇO AV MUTINGA 3800 7º ANDAR PIRITUBA SÃO PAULO FABRICANTE SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH ENDEREÇO REINO UNIDO GLYN RHONWN LLANBERIS CAERNARFON GWYNEDD LL55 4EL UNITED KINGDOM |
| Models | 10345160776 |
| Date | Mar 13, 2015 |
| 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