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ANVISA registration 80021290017Active

Solucao para Preenchimento Intradermico

ANVISA Registration Number: 80021290017CRISTÁLIA PRODUTOS QUÍMICOS FARMACÊUTICOS LTDA.CRISTÁLIA PRODUTOS QUÍMICOS FARMACÊUTICOS LTDA.Risk Class IV
Verified
Device names
Technical name
Solucao para Preenchimento Intradermico
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Commercial name
LUMINAGE MAX
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Risk class
Class IV
Registration details
Registration Number
80021290017
Process Number
25351440172202449
CNPJ
44734671000151
Company information
Registration Holder
CRISTÁLIA PRODUTOS QUÍMICOS FARMACÊUTICOS LTDA.
Manufacturer
CRISTÁLIA PRODUTOS QUÍMICOS FARMACÊUTICOS LTDA.
Manufacturing Country
Brazil
PT: BRASIL
Dates and status
Publication Date
Sep 14, 2026
Status
Active
About this record

Access comprehensive regulatory information for Solucao para Preenchimento Intradermico in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 80021290017 and manufactured by CRISTÁLIA PRODUTOS QUÍMICOS FARMACÊUTICOS LTDA.. The registration is held by CRISTÁLIA PRODUTOS QUÍMICOS FARMACÊUTICOS LTDA. with validity until Sep 14, 2036.

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.