Interbody disc replacement spacer device - ANVISA Registration 80036750025

Access comprehensive regulatory information for Interbody disc replacement spacer device in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80036750025 and manufactured by Bio Engenharia e Indústria de Implantes Ortopédicos Ltda. The registration is held by Bio Engenharia e Indústria de Implantes Ortopédicos Ltda with validity until Sep 23, 2028.

This page provides complete technical specifications for this device, regulatory compliance details, 2 companies making the same product including OTP BIOMÉDICA LTDA, LFC SP. ZO.O, and 4 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.