International safety notice
In vitro Diagnostic Kit
Brazil / Anvisa · BRA · Jul 18, 2013
Key facts
| Title | In vitro Diagnostic Kit |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | ADVIA CENTAUR TSH3-Ultra (TSH3-UL) – Registro Nº 10345161732; FLEX TSH DIMENSION REAGENT - Registration No. 10345161255; TSH THIRD GENERATION IMMULITE/IMMULITE 1000 Registration No. 10345160833; TSH 3rd GENERATION IMMULITE 2000 Registration No. 10345160834 |
| Manufacturer | SIEMENS HEALTHCARE DIAGNOSTICS INC SIEMENS HEALTHCARE DIAGNOSTIC PRODUCTS |
| Models | 10345160834, TSH3-Ultra, 10345161255, TSH3-UL, 10345161732, 10345160833 |
| Date | Jul 18, 2013 |
| 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