Visit us at Medica, Dusseldorf, Germany 17-20 November 2025 at Hall 16, Stand D17-5 and ask us about our free AI tools and the document builder.
Pure Global

Dental Regenerative Membranes - ANVISA Registration 80102512514

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 80102512514 and manufactured by PURGO BIOLOGICS INC.. The registration is held by VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS 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.

Free Database
Powered by Pure Global AI
100,000+ Devices
5 Competitors
5 Recent Registrations
80102512514
Registration Details
ANVISA Registration Number: 80102512514
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

Membrana de PTFE Não Reabsorvível OpenTex®
Risk Class II

Registration Details

80102512514

25351249812202054

04718143000194

Company Information

South Korea
PT: CORÉIA DO SUL

Dates and Status

Jul 20, 2020

VIGENTE

09/18/2025 19:00:01