Anterior column system for interbody fixation - ANVISA Registration 82328860000

Access comprehensive regulatory information for Anterior column system for interbody fixation in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 82328860000 and manufactured by BAUI BIOTECH CO., LTD.. The registration is held by EFFORT PRODUTOS PARA A SAUDE LTDA with validity until Jul 18, 2026.

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 ULRICH GMBH & CO.KG., AESCULAP AG, 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
82328860000
2 Related Devices
Registration Details
ANVISA Registration Number: 82328860000
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)

SISTEMA DE FIXAÇÃO ANTERIOR DE PLACA CERVICAL REBORN ESSENCE
Risk Class III

Registration Details

82328860000

25351237722202282

37323224000144

Company Information

Taiwan
PT: TAIWAN

Dates and Status

Aug 22, 2022

18/07/2026

09/18/2025 19:00:01

SISTEMA DE FIXAÇÃO ANTERIOR DE PLACA CERVICAL REBORN ESSENCE
Risk Class III

Registration Details

82328860000

25351237722202282

37323224000144

Company Information

Dates and Status

Aug 22, 2022

18/07/2026

09/18/2025 19:00:01