Light-Cured Composite Resin - ANVISA Registration 80230400080

Access comprehensive regulatory information for Light-Cured Composite Resin in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80230400080 and manufactured by VOCO GMBH. The registration is held by VOCO DO BRASIL LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including VIGODENT INDUSTRIA E COMERCIO LTDA., VOCO GMBH, 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 Similar Products
5 Competitors
80230400080
Registration Details
ANVISA Registration Number: 80230400080
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

🇧🇷 Brazil Regulatory Expert

Need help with your Brazil registration?

Contact Pure Global Brazil Team
Free consultation

Device Details

Kit GrandioSO Light Flow
Risk Class II

Registration Details

80230400080

25351052363202023

05915452000117

Company Information

VOCO GMBH
Germany
PT: ALEMANHA

Dates and Status

Mar 09, 2020

VIGENTE

09/18/2025 19:00:01