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Cementation Try-In Material - ANVISA Registration 80284930219

Access comprehensive regulatory information for Cementation Try-In Material in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80284930219 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 3 related devices, regulatory compliance details, 5 companies making the same product including IVOCLAR VIVADENT AG, BIODINAMICA QUIMICA E FARMACEUTICA LTDA, 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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80284930219
3 Related Devices
Registration Details
ANVISA Registration Number: 80284930219
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Related Devices (3)

Registration Details

80284930219

25351132234200962

45985371000108

Company Information

3M DO BRASIL LTDA
Brazil
PT: BRASIL

Dates and Status

Aug 31, 2009

VIGENTE

09/18/2025 19:00:01

Registration Details

80284930219

25351132234200962

45985371000108

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMร‰RICA

Dates and Status

Aug 31, 2009

VIGENTE

09/18/2025 19:00:01

Registration Details

80284930219

25351132234200962

45985371000108

Company Information

3M ESPE / AG
Germany
PT: ALEMANHA

Dates and Status

Aug 31, 2009

VIGENTE

09/18/2025 19:00:01