ESOPHAGEAL STENT - ANVISA Registration 80065320301

Access comprehensive regulatory information for ESOPHAGEAL STENT in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80065320301 and manufactured by MI TECH CO., LTD. The registration is held by CMS PRODUTOS HOSPITALARES LTDA with validity until Jan 11, 2031.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including M.I. TECH CO., LTD, MI TECH 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.

Free Database
Powered by Pure Global AI
100,000+ Devices
5 Similar Products
5 Competitors
80065320301
2 Related Devices
Registration Details
ANVISA Registration Number: 80065320301
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

🇧🇷 Brazil Regulatory Expert

Need help with your Brazil registration?

Contact Pure Global Brazil Team
Free consultation

Related Devices (2)

HANAROSTENT® GASTRO-SEALTM ESOFÁGICO (CCC) ECBST
Risk Class III

Registration Details

80065320301

25351073309202011

03301390000128

Company Information

MI TECH CO., LTD
South Korea
PT: CORÉIA DO SUL

Dates and Status

Jan 11, 2021

11/01/2031

09/18/2025 19:00:01

HANAROSTENT® GASTRO-SEALTM ESOFÁGICO (CCC) ECBST
Risk Class III

Registration Details

80065320301

25351073309202011

03301390000128

Company Information

Dates and Status

Jan 11, 2021

11/01/2031

09/18/2025 19:00:01