ANVISA registration 10009010508Valid until Jun 22, 2036

DENGUE

Name: DENGUE — ANVISA registration 10009010508
Creator: LABTEST DIAGNOSTICA S/A
Keywords: DENGUE, DENGUE, Anti-Dengue IgM Reagent Kit, 10009010508, Risk Class III, ANVISA registration

ANVISA Registration Number: 10009010508LABTEST DIAGNOSTICA S/ALABTEST DIAGNOSTICA S/ARisk Class III

Verified

Device names

Technical name: DENGUE
Commercial name: Anti-Dengue IgM Reagent Kit
Risk class: Class III

Registration details

Registration Number: 10009010508
Process Number: 25351007426202682
CNPJ: 16516296000138

Company information

Registration Holder: LABTEST DIAGNOSTICA S/A
Manufacturer: LABTEST DIAGNOSTICA S/A
Manufacturing Country: Brazil

Dates and status

Publication Date: Jun 22, 2026
Validity: 22/06/2036
Last Updated: 08/18/2026 19:00:00

About this record

Access comprehensive regulatory information for DENGUE in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 10009010508 and manufactured by LABTEST DIAGNOSTICA S/A. The registration is held by LABTEST DIAGNOSTICA S/A with validity until Jun 22, 2036.

This page shows the facts attached to this official registry row. Exact-name links return deterministic registry matches; open-ended comparison and market analysis are handed to AI Search with this record's context, without asserting that similar names represent the same entity.