Adhesion/Silanization Agent - ANVISA Registration 10002070027

Access comprehensive regulatory information for Adhesion/Silanization Agent in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10002070027 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 DENTSPLY IND.COM. LTDA, SHOFU INC., 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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10002070027
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Registration Details
ANVISA Registration Number: 10002070027
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

3M ESPE ADPER SCOTCHBOND MULTIUSO PLUS
Risk Class II

Registration Details

10002070027

250000287079618

45985371000108

Company Information

3M DO BRASIL LTDA
Brazil
PT: BRASIL

Dates and Status

Oct 09, 1996

VIGENTE

09/18/2025 19:00:01

3M ESPE ADPER SCOTCHBOND MULTIUSO PLUS
Risk Class II

Registration Details

10002070027

250000287079618

45985371000108

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Oct 09, 1996

VIGENTE

09/18/2025 19:00:01