Visit us at Medica, Dusseldorf, Germany 17-20 November 2025 at Hall 16, Stand D17-5 and ask us about our free AI tools and the document builder.
Pure Global

Anterior column system for interbody fixation - ANVISA Registration 81000030070

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 IV medical device is registered under ANVISA number 81000030070 and manufactured by SPINEART SA. The registration is held by Autentica Medical Importação Comercio e Serviços LTDA-ME with validity until Jul 04, 2026.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 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 Competitors
5 Recent Registrations
81000030070
2 Related Devices
Registration Details
ANVISA Registration Number: 81000030070
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Related Devices (2)

Registration Details

81000030070

25351641952201866

18192496000108

Company Information

SPINEART SA
Switzerland
PT: SUÍÇA

Dates and Status

Oct 01, 2018

04/07/2026

09/18/2025 19:00:01

Registration Details

81000030070

25351641952201866

18192496000108

Dates and Status

Oct 01, 2018

04/07/2026

09/18/2025 19:00:01