International safety notice
Automatic Immunoassay Analyzer/ Physiological Fluid Microorganism Analyzer
Brazil / Anvisa · BRA · Jul 10, 2015
Key facts
| Title | Automatic Immunoassay Analyzer/ Physiological Fluid Microorganism Analyzer |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Immunoassay Analyzers: Immulite 2000XPI System, registration 10345161777 ///// Immulite 1000 System, registration 10345160643 /// Immulite 2000 System, registration 10345160645/// Immulite Automated Immunoassay System 10345161653. The identification of the affected products are listed in Letter in Attachment. |
| Manufacturer | DETENTOR DO REGISTRO SIEMENS HEALTHCARE DIAGNÓSTICOS SA CNPJ 01449930000190 ENDEREÇO AV MUTINGA 3800 5 E 7º ANDAR PIRITUBA SÃO PAULO FABRICANTE SIEMENS HEALTHCARE DIAGNOSTICS INC ENDEREÇO 62 FLANDERS BARTLEY ROAD FLANDERS NJ 07836 ESTADOS UNIDOS |
| Models | 10345160645, 10345160643, 10345161653, 10345161777, 2000XPI |
| Date | Jul 10, 2015 |
| 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