Pure Global AI
ANVISA registration 80638720248Valid until Jun 08, 2036

ANTIBODY FOR HUMAN IMMUNODEFICIENCY VIRUS TYPE 1 AND TYPE 2 (HIV 1 AND HIV 2)

ANVISA Registration Number: 80638720248DIAGNÓSTICA INDÚSTRIA E COMÉRCIO LTDA - MEHANGZHOU ALLTEST BIOTECH CO. LTDRisk Class IV
Device names
Technical name
ANTIBODY FOR HUMAN IMMUNODEFICIENCY VIRUS TYPE 1 AND TYPE 2 (HIV 1 AND HIV 2)
PT: ANTICORPO PARA VÍRUS DE IMUNODEFICIÊNCIA HUMANA TIPO 1 E TIPO 2 (HIV 1 E HIV 2)
Commercial name
HIV 1/2 Rapid Test
Risk class
Class IV
Registration details
Registration Number
80638720248
Process Number
25351013834202673
CNPJ
11462456000190
Company information
Manufacturing Country
China
PT: CHINA, REPÚBLICA POPULAR
Dates and status
Publication Date
Jun 08, 2026
Validity
08/06/2036
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for ANTIBODY FOR HUMAN IMMUNODEFICIENCY VIRUS TYPE 1 AND TYPE 2 (HIV 1 AND HIV 2) in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 80638720248 and manufactured by HANGZHOU ALLTEST BIOTECH CO. LTD. The registration is held by DIAGNÓSTICA INDÚSTRIA E COMÉRCIO LTDA - ME with validity until Jun 08, 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.