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SPINAL FUSION CAGES - ANVISA Registration 80268080018

Access comprehensive regulatory information for SPINAL FUSION CAGES in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80268080018 and manufactured by NOVASPINE S.A.R.L. The registration is held by INTUIT IMPORTAÇÃO E COMÉRCIO DE MATERIAIS CIRÚRGICOS E HOSPITALARES LTDA with validity until Jul 27, 2030.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including AESCULAP AG, OSTEOMED S.A, 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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80268080018
2 Related Devices
Registration Details
ANVISA Registration Number: 80268080018
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Related Devices (2)

CAGE CERVICAL E LOMBAR AUTOBLOQUEANTE DIVA
Risk Class III

Registration Details

80268080018

25351496562201914

05699386000195

Company Information

NOVASPINE S.A.R.L
France
PT: FRANÇA

Dates and Status

Jul 27, 2020

27/07/2030

09/18/2025 19:00:01

CAGE CERVICAL E LOMBAR AUTOBLOQUEANTE DIVA
Risk Class III

Registration Details

80268080018

25351496562201914

05699386000195

Dates and Status

Jul 27, 2020

27/07/2030

09/18/2025 19:00:01