HUMAN CHORIONIC BETA GONADOTROPIN (BHCG) - ANVISA Registration 80638720089
Access comprehensive regulatory information for HUMAN CHORIONIC BETA GONADOTROPIN (BHCG) in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80638720089 and manufactured by GUANG ZHOU WONDFO BIOTECH CO. LTDA. The registration is held by DIAGNÓSTICA INDÚSTRIA E COMÉRCIO LTDA - ME with validity until currently active (VIGENTE).
This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including QUIBASA QUÍMICA BÁSICA LTDA, ABBOTT IRELAND DIAGNOSTICS DIVISION, and 5 recent registrations in the same technical category. Pure Global AI offers free access to over 100,000+ Brazilian medical device registrations, helping global MedTech companies navigate ANVISA regulations, identify competitors, and discover partnership opportunities efficiently.
Device Details
Registration Details
80638720089
25351080585201811
11462456000190
Company Information
Dates and Status
Jun 25, 2018
VIGENTE
09/18/2025 19:00:01
BETA GONADOTROFINA CORIÔNICA HUMANA (BHCG)
ß-HCG FIA Analyzer Test
GUANGZHOU BIOSURPASS BIOTECHNOLOGY CO., LTD
82102680001
Sep 15, 2025
BETA GONADOTROFINA CORIÔNICA HUMANA (BHCG)
FAMÍLIA TESTES DE GRAVIDEZ
RS MED LTDA
80470750009
Aug 18, 2025
BETA GONADOTROFINA CORIÔNICA HUMANA (BHCG)
Luminis FIA ß-HCG Total
QINGDAO HIGHTOP BIOTECH CO.,LTD.
80474870157
Jul 07, 2025
BETA GONADOTROFINA CORIÔNICA HUMANA (BHCG)
BIOCLIN POCT FIA BETA-HCG
QUIBASA QUÍMICA BÁSICA LTDA
10269360469
Jun 09, 2025
BETA GONADOTROFINA CORIÔNICA HUMANA (BHCG)
Família Cassete de Teste ß -hCG (Sangue Total/Soro/Plasma)
ACRO BIOTECH, INC. (MONTCLAIR)
81325990388
Jun 02, 2025

