Light-Cured Composite Resin - ANVISA Registration 80284930313

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 80284930313 and manufactured by 3M do Brasil Ltda. The registration is held by 3M DO BRASIL LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for 2 related devices, 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.

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80284930313
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Registration Details
ANVISA Registration Number: 80284930313
Janaina dos Santos de Miranda

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Related Devices (2)

3M ESPE FILTEK BULK FILL FLOW RESINA EM BULK DE BAIXA CONTRAÇÃO
Risk Class II

Registration Details

80284930313

25351329351201371

45985371000108

Company Information

3M do Brasil Ltda
Brazil
PT: BRASIL

Dates and Status

Jul 28, 2014

VIGENTE

09/18/2025 19:00:01

3M ESPE FILTEK BULK FILL FLOW RESINA EM BULK DE BAIXA CONTRAÇÃO
Risk Class II

Registration Details

80284930313

25351329351201371

45985371000108

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Jul 28, 2014

VIGENTE

09/18/2025 19:00:01