SPINAL FUSION CAGES - ANVISA Registration 80102511114

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 80102511114 and manufactured by SEASPINE ORTHOPEDICS CORPORATION. The registration is held by VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDA with validity until Mar 25, 2028.

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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80102511114
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Registration Details
ANVISA Registration Number: 80102511114
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

ESPAÇADOR VERTEBRAL CAMBRIA
Risk Class III

Registration Details

80102511114

25351332049201043

04718143000194

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Mar 25, 2013

25/03/2028

09/18/2025 19:00:01

ESPAÇADOR VERTEBRAL CAMBRIA
Risk Class III

Registration Details

80102511114

25351332049201043

04718143000194

Dates and Status

Mar 25, 2013

25/03/2028

09/18/2025 19:00:01