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Facial Implant - ANVISA Registration 80094170105

Access comprehensive regulatory information for Facial Implant in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80094170105 and manufactured by manufacturer not specified. The registration is held by INTERMEDIC TECHNOLOGY IMPORTACAO E EXPORTACAO LTDA with validity until Jun 28, 2031.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including MATRIX SURGICAL USA, Sistema de Implantes Nacionais e de Próteses Comércio 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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80094170105
2 Related Devices
Registration Details
ANVISA Registration Number: 80094170105
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Related Devices (2)

Implantes Orbitais Omnipore® Duromax®
Risk Class III

Registration Details

80094170105

25351077302202079

01390500000140

Company Information

Dates and Status

Jun 28, 2021

28/06/2031

09/18/2025 19:00:01

Implantes Orbitais Omnipore® Duromax®
Risk Class III

Registration Details

80094170105

25351077302202079

01390500000140

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Jun 28, 2021

28/06/2031

09/18/2025 19:00:01