International safety notice
ACTIVATED PARTIAL THROMBOPLASTIN TIME (APTT)
Brazil / Anvisa · BRA · Apr 13, 2015
Key facts
| Title | ACTIVATED PARTIAL THROMBOPLASTIN TIME (APTT) |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Actin® Activated Cephaloplastin Reagent, Packaging of 2 x 10 ml - Registration 10345161140 - lots 557128; |
| Manufacturer | DETENTOR DO REGISTRO NO BRASIL SIEMENS HEALTHCARE DIAGNÓSTICOS LTDA CNPJ 01449930000190 ENDEREÇO AV MUTINGA 3800 7º ANDAR PIRITUBA SÃO PAULO SÃO PAULO TELEFONE 11 39083860 |
| Models | 10345161140, 557131, 557128, 557135 |
| Date | Apr 13, 2015 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models 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