ANVISA registration 80065320295Valid until Aug 31, 2030NON-VASCULAR STENT (NOT CLASSIFIED AS BILIARY, BRONCHIAL, ESOPHAGEAL, PANCREATIC, URINARY AND VAGINAL)
ANVISA Registration Number: 80065320295CMS PRODUTOS HOSPITALARES LTDAMI TECH CO., LTDRisk Class III
Device names
- Technical name
- NON-VASCULAR STENT (NOT CLASSIFIED AS BILIARY, BRONCHIAL, ESOPHAGEAL, PANCREATIC, URINARY AND VAGINAL)
- Commercial name
- HANAROSTENT® LOWAX Duodenal/Pilórico (NNN) DNJF (APLICAÇÃO ENDOSCÓPICA)
- Risk class
- Class III
PT: STENT NÃO VASCULAR (NÃO ENQUADRADO COMO BILIAR, BRONQUIAL, ESOFÁGICO, PANCREÁTICO, URINÁRIO E VAGINAL)
Registration details
- Registration Number
- 80065320295
- Process Number
- 25351749123201910
- CNPJ
- 03301390000128
Company information
- Registration Holder
- CMS PRODUTOS HOSPITALARES LTDA
- Manufacturer
- MI TECH CO., LTD
- Manufacturing Country
- South Korea
PT: CORÉIA DO SUL
Dates and status
- Publication Date
- Aug 31, 2020
- Validity
- 31/08/2030
- 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 80065320295 and manufactured by MI TECH CO., LTD. The registration is held by CMS PRODUTOS HOSPITALARES LTDA with validity until Aug 31, 2030.
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