SPINAL FUSION CAGES - ANVISA Registration 80268080018
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 80268080018 and manufactured by NOVASPINE S.A.R.L. The registration is held by INTUIT IMPORTAÇÃO E COMÉRCIO DE MATERIAIS CIRÚRGICOS E HOSPITALARES LTDA with validity until Jul 27, 2030.
This page provides complete technical specifications for 2 related devices, regulatory compliance details, 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.
Related Devices (2)
Registration Details
80268080018
25351496562201914
05699386000195
Company Information
Dates and Status
Jul 27, 2020
27/07/2030
09/18/2025 19:00:01
CAGES PARA FUSÃO DE COLUNA
DISPOSITIVO INTERSOMÁTICO LLIF OSTEO FUSION EM PEEK
OSTEOMED S.A
80071910131
Jun 30, 2025
CAGES PARA FUSÃO DE COLUNA
E.CROSS A
EUROS S.A.S.
80770610012
Jun 30, 2025
CAGES PARA FUSÃO DE COLUNA
E.CROSS A
Not specified
80770610012
Jun 30, 2025
CAGES PARA FUSÃO DE COLUNA
CAGE PEEK P – VIA POSTERIOR
JIANGSU TRAUHUI MEDICAL INSTRUMENT CO LTD
81660180003
Mar 31, 2025
CAGES PARA FUSÃO DE COLUNA
CAGE PEEK P – VIA POSTERIOR
Not specified
81660180003
Mar 31, 2025

