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SPINAL FUSION CAGES - ANVISA Registration 80528190053

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 80528190053 and manufactured by Normmed Medikal VE Makina Sanayi Ticaret Limited Sirketi. The registration is held by NEUROCIÊNCIAS COMÉRCIO E LOCAÇÃO DE PRODUTOS MÉDICOS LTDA with validity until Aug 16, 2031.

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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80528190053
2 Related Devices
Registration Details
ANVISA Registration Number: 80528190053
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Related Devices (2)

Dispositivo Intersomático Lombar Anterior em PEEK – ALIF Normmed
Risk Class III

Registration Details

80528190053

25351090913202011

07764288000110

Company Information

Dates and Status

Aug 16, 2021

16/08/2031

09/18/2025 19:00:01

Dispositivo Intersomático Lombar Anterior em PEEK – ALIF Normmed
Risk Class III

Registration Details

80528190053

25351090913202011

07764288000110

Dates and Status

Aug 16, 2021

16/08/2031

09/18/2025 19:00:01