Dental Regenerative Membranes - ANVISA Registration 80696930012

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 provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including Bone Heal Indústria e Comércio Ltda, OSTEOGENICS BIOMEDICAL, INC., and 5 recent registrations in the same technical category. Pure Global AI offers free access to over 100,000+ Brazilian medical device registrations, helping global MedTech companies navigate ANVISA regulations, identify competitors, and discover partnership opportunities efficiently.