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ANVISA registration 80524900007Active

FOLLICLE STIMULATING HORMONE (FSH)

ANVISA Registration Number: 80524900007BIO ADVANCE DIAGNOSTICOS LTDAPISHTAZ TEB ZAMAN DIAGNOSTICS CORisk Class II
Verified
Device names
Technical name
FOLLICLE STIMULATING HORMONE (FSH)
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PT: HORMÔNIO FOLÍCULO ESTIMULANTE (FSH)
Commercial name
Kit ELISA FSH
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Risk class
Class II
Registration details
Registration Number
80524900007
Process Number
25351594818200968
CNPJ
09593438000103
Company information
Registration Holder
BIO ADVANCE DIAGNOSTICOS LTDA
Manufacturer
PISHTAZ TEB ZAMAN DIAGNOSTICS CO
Manufacturing Country
Iran
PT: IRÃ
Dates and status
Publication Date
Mar 08, 2010
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for FOLLICLE STIMULATING HORMONE (FSH) in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80524900007 and manufactured by PISHTAZ TEB ZAMAN DIAGNOSTICS CO. The registration is held by BIO ADVANCE DIAGNOSTICOS 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.