SPINAL FUSION CAGES - ANVISA Registration 80071910032

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 80071910032 and manufactured by OSTEOMED S.A. The registration is held by OSTEOMED S.A with validity until Jan 05, 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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80071910032
Registration Details
ANVISA Registration Number: 80071910032
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Device Details

DIPOSITIVO INTERSOMÁTICO TRANFORAMINAL - TLIF PEEK
Risk Class IV

Registration Details

80071910032

25351501144201237

00638390000120

Company Information

OSTEOMED S.A
Brazil
PT: BRASIL

Dates and Status

Jan 05, 2015

05/01/2035

09/18/2025 19:00:01