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ANVISA registration 80251760013Valid until Feb 28, 2036

Solution for Intradermal Filling

ANVISA Registration Number: 80251760013GALDERMA BRASIL LTDAQ-MED ABRisk Class IV
Verified
Device names
Technical name
Solution for Intradermal Filling
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PT: Solucao para Preenchimento Intradermico
Commercial name
Restylane Kysse
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Risk class
Class IV
Registration details
Registration Number
80251760013
Process Number
25351729366201586
CNPJ
00317372000146
Company information
Registration Holder
GALDERMA BRASIL LTDA
Manufacturer
Q-MED AB
Manufacturing Country
Sweden
PT: SUÉCIA
Dates and status
Publication Date
Feb 29, 2016
Validity
28/02/2036
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for Solution for Intradermal Filling in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 80251760013 and manufactured by Q-MED AB. The registration is held by GALDERMA BRASIL LTDA with validity until Feb 28, 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.