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ANVISA registration 80048490102Active

DEHYDROEPIANDROSTERONE (DHEA)

ANVISA Registration Number: 80048490102USA DIAGNOSTICA LTDAMONOBIND, INCRisk Class II
Verified
Device names
Technical name
DEHYDROEPIANDROSTERONE (DHEA)
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PT: DEHIDROEPIANDROSTERONA (DHEA)
Commercial name
DHEA Test System – ELISA
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Risk class
Class II
Registration details
Registration Number
80048490102
Process Number
25351413649202413
CNPJ
02330159000108
Company information
Registration Holder
USA DIAGNOSTICA LTDA
Manufacturer
MONOBIND, INC
Manufacturing Country
United States
PT: ESTADOS UNIDOS DA AMÉRICA
Dates and status
Publication Date
Dec 23, 2024
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for DEHYDROEPIANDROSTERONE (DHEA) in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80048490102 and manufactured by MONOBIND, INC. The registration is held by USA DIAGNOSTICA 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.