Console Nucleotome

Discectomy surgical equipment · class III · Until 10/04/2027

Registration no.
80109170024
Process no.
25351517923201529
Status
Until 10/04/2027
Device type
Discectomy surgical equipment (Equipamento Cirurgico para Discectomia)
Risk class
III
Registration holder
MEM CIRURGICA LTDA. CNPJ 04.733.376/0001-66 · 49 registrations
Manufacturer
CLARUS MEDICAL, LLC · United States
Published
10/04/2017
Valid until
10/04/2027
Last updated by ANVISA
2026-10-12
Official record
View on ANVISA ↗

Other discectomy surgical equipment registrations (17 in total, see all)

ProductClass HolderPublishedStatus
Kit RRM Standard +
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III MARDEN MEDICAL LTDA 05/03/2025 Until 05/03/2035
Kit Discectomia Percutânea Disc Pró +
82209520029
III MARDEN MEDICAL LTDA 05/03/2025 Until 05/03/2035
Kit Scraper Fast Marden +
82209520030
III MARDEN MEDICAL LTDA 05/03/2025 Until 05/03/2035
Kit Cânula Percutaneous Endoscopy Marden +
82209520031
III MARDEN MEDICAL LTDA 05/03/2025 Until 05/03/2035
Kit Scraper Plus Marden +
82209520036
III MARDEN MEDICAL LTDA 05/03/2025 Until 05/03/2035
Kit Scraper Duo Marden +
82209520037
III MARDEN MEDICAL LTDA 05/03/2025 Until 05/03/2035
Kit Cânula de Descompressão Endoscópica Dirigível Orthodisc +
82209520038
III MARDEN MEDICAL LTDA 05/03/2025 Until 05/03/2035
Kit Cânula CurActive Discovery Plus Safedisc
82603640001
III MEDFACTOR INDUSTRIA E COMERCIO DE PRODUTOS MEDICOS HOSPITALARES LTDA 09/12/2024 Until 09/12/2034