Surgical Equipment for Discectomy - ANVISA Registration 81050769011
Access comprehensive regulatory information for Surgical Equipment for Discectomy in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81050769011 and manufactured by BIOPSYBELL S.R.L.. The registration is held by GUSMED DO BRASIL COMERCIO E LOCAÇÃO DE PRODUTOS MEDICOS LTDA - EPP with validity until currently active (VIGENTE).
This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including MARDEN MEDICAL LTDA, SEAWON MEDITECH CO., LTD, 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.
Device Details
Registration Details
81050769011
25351821648202104
19443457000107
Company Information
Dates and Status
Jan 14, 2021
VIGENTE
09/18/2025 19:00:01
Equipamento Cirurgico para Discectomia
Kit RRM Standard +
MARDEN MEDICAL LTDA
82209520028
Mar 05, 2025
Equipamento Cirurgico para Discectomia
Kit Discectomia Percutânea Disc Pró +
MARDEN MEDICAL LTDA
82209520029
Mar 05, 2025
Equipamento Cirurgico para Discectomia
Kit Scraper Fast Marden +
MARDEN MEDICAL LTDA
82209520030
Mar 05, 2025
Equipamento Cirurgico para Discectomia
Kit Cânula Percutaneous Endoscopy Marden +
MARDEN MEDICAL LTDA
82209520031
Mar 05, 2025
Equipamento Cirurgico para Discectomia
Kit Scraper Plus Marden +
MARDEN MEDICAL LTDA
82209520036
Mar 05, 2025

