SPINAL FUSION CAGES - ANVISA Registration 80102512115

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 80102512115 and manufactured by MEDACTA INTERNATIONAL S.A.. The registration is held by VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDA with validity until Sep 24, 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.

Free Database
Powered by Pure Global AI
100,000+ Devices
5 Similar Products
5 Competitors
80102512115
2 Related Devices
Registration Details
ANVISA Registration Number: 80102512115
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

🇧🇷 Brazil Regulatory Expert

Need help with your Brazil registration?

Contact Pure Global Brazil Team
Free consultation

Related Devices (2)

DISPOSITIVOS DE FUSÃO INTERVERTEBRALMECTALIF REVESTIDO
Risk Class III

Registration Details

80102512115

25351275731201895

04718143000194

Company Information

Switzerland
PT: SUÍÇA

Dates and Status

Sep 24, 2018

24/09/2028

09/18/2025 19:00:01

DISPOSITIVOS DE FUSÃO INTERVERTEBRALMECTALIF REVESTIDO
Risk Class III

Registration Details

80102512115

25351275731201895

04718143000194

Dates and Status

Sep 24, 2018

24/09/2028

09/18/2025 19:00:01