Light-Cured Composite Resin - ANVISA Registration 80284930215
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 80284930215 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.

Janaina dos Santos de Miranda
🇧🇷 Brazil Regulatory Expert
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Contact Pure Global Brazil TeamRelated Devices (2)
Registration Details
80284930215
25351236757200846
45985371000108
Company Information
Dates and Status
Dec 22, 2008
VIGENTE
09/18/2025 19:00:01
Registration Details
80284930215
25351236757200846
45985371000108
Company Information
Dates and Status
Dec 22, 2008
VIGENTE
09/18/2025 19:00:01
Light-Cured Composite Resin
3M ESPE FILTEK Z350 XT RESTAURADOR UNIVERSAL
3M DO BRASIL LTDA
80284930233
Apr 30, 2010
Light-Cured Composite Resin
3M ESPE FILTEK Z350 XT RESTAURADOR UNIVERSAL
3 M ESPE DENTAL PRODUCTS
80284930233
Apr 30, 2010
Light-Cured Composite Resin
3M ESPE FILTEK Z350 XT RESTAURADOR UNIVERSAL
3M COMPANY - 3M ESPE DENTAL PRODUCTS
80284930233
Apr 30, 2010
Light-Cured Composite Resin
3M ESPE FILTEK Z250 XT RESTAURADOR UNIVERSAL
3M ESPE AG
80284930263
Sep 26, 2011
Light-Cured Composite Resin
3M ESPE FILTEK Z250 XT RESTAURADOR UNIVERSAL
3M ESPE DENTAL PRODUCTS
80284930263
Sep 26, 2011
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