SPINAL FUSION CAGES - ANVISA Registration 80071910131

Access comprehensive regulatory information for SPINAL FUSION CAGES in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 80071910131 and manufactured by OSTEOMED S.A. The registration is held by OSTEOMED S.A with validity until Jun 30, 2035.

This page provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including AESCULAP AG, MEDACTA INTERNATIONAL 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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80071910131
Registration Details
ANVISA Registration Number: 80071910131
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Device Details

DISPOSITIVO INTERSOMÁTICO LLIF OSTEO FUSION EM PEEK
Risk Class IV

Registration Details

80071910131

25351200789202423

00638390000120

Company Information

OSTEOMED S.A
Brazil
PT: BRASIL

Dates and Status

Jun 30, 2025

30/06/2035

09/18/2025 19:00:01