INTERNAL VERTEBRAL COLUMN FIXATION SYSTEMS - ANVISA Registration 10349000902

Access comprehensive regulatory information for INTERNAL VERTEBRAL COLUMN FIXATION SYSTEMS in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 10349000902 and manufactured by MEDTRONIC SOFAMOR DANEK USA, INC. The registration is held by AUTO SUTURE DO BRASIL LTDA. with validity until Apr 27, 2035.

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 MEDTRONIC SOFAMOR DANEK USA, INC, GLOBUS MEDICAL, 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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10349000902
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Registration Details
ANVISA Registration Number: 10349000902
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Related Devices (2)

SISTEMA DE RECONSTRUÇÃO POSTERIOR DA COLUNA VERTEX MAX®
Risk Class IV

Registration Details

10349000902

25351375647202095

01645409000128

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Jun 01, 2020

27/04/2035

09/18/2025 19:00:01

SISTEMA DE RECONSTRUÇÃO POSTERIOR DA COLUNA VERTEX MAX®
Risk Class IV

Registration Details

10349000902

25351375647202095

01645409000128

Company Information

Dates and Status

Jun 01, 2020

27/04/2035

09/18/2025 19:00:01