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ANVISA registration 80696930012Valid until May 27, 2029

Dental Regenerative Membranes

ANVISA Registration Number: 80696930012GEISTLICH PHARMA DO BRASIL COMERCIO E SERVIÇOS DE PRODUTOS PARA SAUDE LTDAGEISTLICH PHARMA AGRisk Class IV
Verified
Device names
Technical name
Dental Regenerative Membranes
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PT: Membranas Regenerativas Odontologicas
Commercial name
GEISTLICH FIBRO-GIDE®
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Risk class
Class IV
Registration details
Registration Number
80696930012
Process Number
25351698201201811
CNPJ
11344677000163
Company information
Registration Holder
GEISTLICH PHARMA DO BRASIL COMERCIO E SERVIÇOS DE PRODUTOS PARA SAUDE LTDA
Manufacturer
GEISTLICH PHARMA AG
Manufacturing Country
Switzerland
PT: SUÍÇA
Dates and status
Publication Date
May 27, 2019
Validity
27/05/2029
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for Dental Regenerative Membranes in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 80696930012 and manufactured by GEISTLICH PHARMA AG. The registration is held by GEISTLICH PHARMA DO BRASIL COMERCIO E SERVIÇOS DE PRODUTOS PARA SAUDE LTDA with validity until May 27, 2029.

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.