ANVISA registration

FT3 Reagent Kit

Registration 10009010419. TRIIODOTIRONINA (T3) LIVRE

Registration details

Registration number10009010419
Application number25351856914202373
Technical nameTRIIODOTIRONINA (T3) LIVRE
Risk classII
Published on15/01/2024
ValidityIndefinite validity

Registration holder

Legal nameLABTEST DIAGNOSTICA S/A
CNPJ16.516.296/0001-38

Manufacturer

  • LABTEST DIAGNOSTICA S/A BRASIL

Source: ANVISA

Source: 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