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ANVISA registration 80696930011Valid until Dec 15, 2034

Regenerative Membranes

ANVISA Registration Number: 80696930011GEISTLICH PHARMA DO BRASIL COMERCIO E SERVIÇOS DE PRODUTOS PARA SAUDE LTDAGEISTLICH PHARMA AGRisk Class IV
Verified
Device names
Technical name
Regenerative Membranes
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PT: Membranas Regeneradoras
Commercial name
CHONDRO GIDE®
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Risk class
Class IV
Registration details
Registration Number
80696930011
Process Number
25351282512201241
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
Dec 15, 2014
Validity
15/12/2034
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for 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 80696930011 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 Dec 15, 2034.

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.