Surgical Equipment for Discectomy - ANVISA Registration 82209520029
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 82209520029 and manufactured by MARDEN MEDICAL LTDA. The registration is held by MARDEN MEDICAL LTDA with validity until Mar 05, 2035.
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
82209520029
25351457113202418
40220751000138
Company Information
Dates and Status
Mar 05, 2025
05/03/2035
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 Scraper Fast Marden +
MARDEN MEDICAL LTDA
82209520030
Mar 05, 2025
Equipamento Cirurgico para Discectomia
Kit Cรขnula 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
Equipamento Cirurgico para Discectomia
Kit Scraper Duo Marden +
MARDEN MEDICAL LTDA
82209520037
Mar 05, 2025

