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ANVISA registration 80002670092Active

SELF-TEST FOR HUMAN CHORIONIC GONADOTROPIN (HCG)

ANVISA Registration Number: 80002670092RENYLAB QUÍMICA E FARMACÊUTICA LTDAINNOVITA (TANGSHAN) BIOLOGICAL TECHNOLOGY CO., LTDRisk Class II
Verified
Device names
Technical name
SELF-TEST FOR HUMAN CHORIONIC GONADOTROPIN (HCG)
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PT: AUTOTESTE PARA GONADOTROFINA CORIÔNICA HUMANA (HCG)
Commercial name
FAMIVITA TESTE DE GRAVIDEZ
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Risk class
Class II
Registration details
Registration Number
80002670092
Process Number
25351559266201602
CNPJ
00562583000144
Company information
Registration Holder
RENYLAB QUÍMICA E FARMACÊUTICA LTDA
Manufacturer
INNOVITA (TANGSHAN) BIOLOGICAL TECHNOLOGY CO., LTD
Manufacturing Country
China
PT: CHINA, REPÚBLICA POPULAR
Dates and status
Publication Date
Mar 27, 2017
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for SELF-TEST FOR HUMAN CHORIONIC GONADOTROPIN (HCG) in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80002670092 and manufactured by INNOVITA (TANGSHAN) BIOLOGICAL TECHNOLOGY CO., LTD. The registration is held by RENYLAB QUÍMICA E FARMACÊUTICA LTDA with validity until currently active (VIGENTE).

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.