Pure Global AI
ANVISA registration 80065320300Valid until Dec 14, 2030

NON-VASCULAR STENT (NOT CLASSIFIED AS BILIARY, BRONCHIAL, ESOPHAGEAL, PANCREATIC, URINARY AND VAGINAL)

ANVISA Registration Number: 80065320300CMS PRODUTOS HOSPITALARES LTDAM.I. TECH CO., LTDRisk Class III
Device names
Technical name
NON-VASCULAR STENT (NOT CLASSIFIED AS BILIARY, BRONCHIAL, ESOPHAGEAL, PANCREATIC, URINARY AND VAGINAL)
PT: STENT NÃO VASCULAR (NÃO ENQUADRADO COMO BILIAR, BRONQUIAL, ESOFÁGICO, PANCREÁTICO, URINÁRIO E VAGINAL)
Commercial name
HANAROSTENT® LOWAX™ COLO/RETAL (NNN) CNJF – APLICAÇÃO ENDOSCÓPICA
Risk class
Class III
Registration details
Registration Number
80065320300
Process Number
25351867413202070
CNPJ
03301390000128
Company information
Manufacturing Country
South Korea
PT: CORÉIA DO SUL
Dates and status
Publication Date
Dec 14, 2020
Validity
14/12/2030
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for NON-VASCULAR STENT (NOT CLASSIFIED AS BILIARY, BRONCHIAL, ESOPHAGEAL, PANCREATIC, URINARY AND VAGINAL) in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80065320300 and manufactured by M.I. TECH CO., LTD. The registration is held by CMS PRODUTOS HOSPITALARES LTDA with validity until Dec 14, 2030.

This page shows the facts attached to this official registry row. Exact-name links return deterministic registry matches; open-ended comparison and market analysis are handed to AI Search with this record's context, without asserting that similar names represent the same entity.