SPINAL FUSION CAGES - ANVISA Registration 80444810055
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 80444810055 and manufactured by manufacturer not specified. The registration is held by HIGHRIDGE MEDICAL BRASIL LTDA with validity until Jun 14, 2031.
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
80444810055
25351373109202066
08954683000128
Company Information
Dates and Status
Jun 14, 2021
14/06/2031
09/18/2025 19:00:01
CAGES PARA FUSรO DE COLUNA
DISPOSITIVO INTERSOMรTICO LLIF OSTEO FUSION EM PEEK
OSTEOMED S.A
80071910131
Jun 30, 2025
CAGES PARA FUSรO DE COLUNA
E.CROSS A
EUROS S.A.S.
80770610012
Jun 30, 2025
CAGES PARA FUSรO DE COLUNA
E.CROSS A
Not specified
80770610012
Jun 30, 2025
CAGES PARA FUSรO DE COLUNA
CAGE PEEK P โ VIA POSTERIOR
JIANGSU TRAUHUI MEDICAL INSTRUMENT CO LTD
81660180003
Mar 31, 2025
CAGES PARA FUSรO DE COLUNA
CAGE PEEK P โ VIA POSTERIOR
Not specified
81660180003
Mar 31, 2025

