ANVISA registration
Família Centrífuga CF-260
Registration 10298910183. Instrumento para preparo e processamento de amostras fase pré-analítica
Registration details
| Registration number | 10298910183 |
|---|---|
| Application number | 25351387280202486 |
| Technical name | Instrumento para preparo e processamento de amostras fase pré-analítica |
| Risk class | I |
| Published on | 16/09/2024 |
| Validity | Indefinite validity |
Registration holder
| Legal name | REVVITY DO BRASIL LTDA |
|---|---|
| CNPJ | 00.351.210/0001-24 |
Manufacturer
- OMNI INTERNATIONAL, INC ESTADOS UNIDOS DA AMÉRICA
Other registrations held by REVVITY DO BRASIL LTDAview all
FAMÍLIA DE KITS DELFIA/AUTODELFIA T4 NEONATAL TIROXINA
10298910003FAMÍLIA DE KITS DELFIA/AUTODELFIA TSH NEONATAL TIROTROPINA
10298910010KIT DELFIA AUTODELFIA 17 ALFA-HIDROXIPROGESTERONA NEONATAL
10298910015FAMÍLIA DE KITS DELFIA/AUTODELFIA IRT NEONATAL TRIPSINA IMUNOREATIVA
10298910032SOLUCAO DE LAVAGEM CONCENTRADA DELFIA
10298910033SOLUÇÃO ENHANCEMENT DELFIA
10298910034Source: ANVISA open data, medical device file, updated daily. The public database provides registration validity, rather than registration status: this registration may have been cancelled before its expiry date without this being shown here. Before making purchasing, import or marketing decisions, check the ANVISA search portal.
Next step
Medical device registration with ANVISA
HSC manages the process from risk classification to liaising with the regulator, in Brazil and more than 40 other countries.
Speak to a specialist