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ANVISA registration 81353340005Active

Guia

ANVISA Registration Number: 81353340005Bio Architects Desenvolvimento de Materiais Especiais LtdaBio Architects Desenvolvimento de Materiais Especiais LtdaRisk Class I
Verified
Device names
Technical name
Guia
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Commercial name
Re•Mold Face Sculpt
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Risk class
Class I
Registration details
Registration Number
81353340005
Process Number
25351225304202595
CNPJ
21522094000139
Company information
Registration Holder
Bio Architects Desenvolvimento de Materiais Especiais Ltda
Manufacturer
Bio Architects Desenvolvimento de Materiais Especiais Ltda
Manufacturing Country
Brazil
PT: BRASIL
Dates and status
Publication Date
Jan 05, 2026
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for Guia in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 81353340005 and manufactured by Bio Architects Desenvolvimento de Materiais Especiais Ltda. The registration is held by Bio Architects Desenvolvimento de Materiais Especiais 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.