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Instrumental for Spine Implant - ANVISA Registration 80263059003

Access comprehensive regulatory information for Instrumental for Spine Implant in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80263059003 and manufactured by ALPHATEC SPINE INC.. The registration is held by GLOBUS MEDICAL BRASIL LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 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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80263059003
2 Related Devices
Registration Details
ANVISA Registration Number: 80263059003
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Related Devices (2)

Kit instrumental para Gaiola de Fixaรงรฃo Lombar Scient 'X
Risk Class I

Registration Details

80263059003

25351640064201143

07131437000103

Company Information

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

Dates and Status

Feb 27, 2012

VIGENTE

09/18/2025 19:00:01

Kit instrumental para Gaiola de Fixaรงรฃo Lombar Scient 'X
Risk Class I

Registration Details

80263059003

25351640064201143

07131437000103

Company Information

SCIENTยดX
France
PT: FRANร‡A

Dates and Status

Feb 27, 2012

VIGENTE

09/18/2025 19:00:01