SPINAL FUSION CAGES - ANVISA Registration 81050760089

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 81050760089 and manufactured by NOVAX DMA S.A. The registration is held by GUSMED DO BRASIL COMERCIO E LOCAÇÃO DE PRODUTOS MEDICOS LTDA - EPP with validity until Oct 14, 2029.

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 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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81050760089
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Registration Details
ANVISA Registration Number: 81050760089
Janaina dos Santos de Miranda

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Related Devices (2)

CAGES PARA FUSÃO INTERSOMÁTICA LOMBAR POR VIA LATERAL MINIMAMENTE INVASIVA – XLIF NOVAX DMA
Risk Class III

Registration Details

81050760089

25351510967201964

19443457000107

Company Information

NOVAX DMA S.A
Argentina
PT: ARGENTINA

Dates and Status

Oct 14, 2019

14/10/2029

09/18/2025 19:00:01

CAGES PARA FUSÃO INTERSOMÁTICA LOMBAR POR VIA LATERAL MINIMAMENTE INVASIVA – XLIF NOVAX DMA
Risk Class III

Registration Details

81050760089

25351510967201964

19443457000107

Dates and Status

Oct 14, 2019

14/10/2029

09/18/2025 19:00:01