Surgical Equipment for Discectomy - ANVISA Registration 80109170024
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 III medical device is registered under ANVISA number 80109170024 and manufactured by CLARUS MEDICAL, LLC. The registration is held by MEM CIRURGICA LTDA. with validity until Apr 10, 2027.
This page provides complete technical specifications for 2 related devices, 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.
Related Devices (2)
Registration Details
80109170024
25351517923201529
04733376000166
Company Information
Dates and Status
Apr 10, 2017
10/04/2027
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

