Graft-carrying diaphyseal spacer cage - ANVISA Registration 80218010019
Access comprehensive regulatory information for Graft-carrying diaphyseal spacer cage in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80218010019 and manufactured by manufacturer not specified. The registration is held by ORTOMEDIC DISTRIBUIDORA DE PRODUTOS MEDICOS LTDA with validity until Jul 14, 2028.
This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search, 1 companies making the same product including SPINEVISION S.A, and 2 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.

Janaina dos Santos de Miranda
🇧🇷 Brazil Regulatory Expert
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Contact Pure Global Brazil TeamRelated Devices (2)
Registration Details
80218010019
25351039953200874
65564536000185
Company Information
Dates and Status
Jul 14, 2008
14/07/2028
09/18/2025 19:00:01
BONE GRAFT AND ASSOCIATED DEVICES
ENXERTO ÓSSEO ACTIFUSE™
Not specified
80253610018
Feb 28, 2011
BONE GRAFT AND ASSOCIATED DEVICES
ENXERTO ÓSSEO ACTIFUSE™
APATECH LIMITED
80253610018
Feb 28, 2011
BONE GRAFT AND ASSOCIATED DEVICES
ORTHOSS®
Not specified
80696930008
Oct 06, 2014
BONE GRAFT AND ASSOCIATED DEVICES
ORTHOSS®
GEISTLICH PHARMA AG
80696930008
Oct 06, 2014
BONE GRAFT AND ASSOCIATED DEVICES
TCH®
Not specified
80686360208
Feb 11, 2019
Cesta espaçadora diafisária carreadora de enxerto
Spacevision™ PLIF
SPINEVISION S.A
80218010017
Jul 14, 2008
Cesta espaçadora diafisária carreadora de enxerto
Spacevision™ PLIF
Not specified
80218010017
Jul 14, 2008