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Dental Regenerative Membranes - ANVISA Registration 80117580161

Access comprehensive regulatory information for Dental Regenerative Membranes in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80117580161 and manufactured by osteogenics biomedical, inc. The registration is held by EMERGO BRAZIL IMPORT IMPORTACAO E DISTRIBUICAO DE PRODUTOS MEDICOS HOSPITALARES LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including Bone Heal Indústria e Comércio Ltda, GEISTLICH PHARMA AG, 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.

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80117580161
Registration Details
ANVISA Registration Number: 80117580161
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Device Details

Cytoplast Regentex Non-Resorbable Barrier Membranes
Risk Class II

Registration Details

80117580161

25351106091201216

04967408000198

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Mar 25, 2013

VIGENTE

09/18/2025 19:00:01