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ANVISA registration 81327670139Active

PROGESTERONE

ANVISA Registration Number: 81327670139DNEDX COMERCIO E SERVICOS PARA PRODUTOS DA SAUDE LTDALANSION BIOTECHNOLOGY CO., LTD.Risk Class II
Verified
Device names
Technical name
PROGESTERONE
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PT: PROGESTERONA
Commercial name
LS – PROGESTERONA TEST
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Risk class
Class II
Registration details
Registration Number
81327670139
Process Number
25351194634202360
CNPJ
22940751000120
Company information
Registration Holder
DNEDX COMERCIO E SERVICOS PARA PRODUTOS DA SAUDE LTDA
Manufacturer
LANSION BIOTECHNOLOGY CO., LTD.
Manufacturing Country
China
PT: CHINA, REPÚBLICA POPULAR
Dates and status
Publication Date
May 02, 2023
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for PROGESTERONE in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81327670139 and manufactured by LANSION BIOTECHNOLOGY CO., LTD.. The registration is held by DNEDX COMERCIO E SERVICOS PARA PRODUTOS DA SAUDE 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.