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ESOPHAGEAL STENT - ANVISA Registration 81040530082

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 81040530082 and manufactured by manufacturer not specified. The registration is held by PROSURGERY- IMPORTAÇÃO E COMÉRCIO DE MATERIAL CIRÚRGICO LTDA ME with validity until Jan 11, 2031.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 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.

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81040530082
2 Related Devices
Registration Details
ANVISA Registration Number: 81040530082
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Related Devices (2)

Prótese Esofágica Revestida Niti-S™ Anti-Refluxo
Risk Class III

Registration Details

81040530082

25351266084202045

13179728000174

Dates and Status

Jan 11, 2021

11/01/2031

09/18/2025 19:00:01

Prótese Esofágica Revestida Niti-S™ Anti-Refluxo
Risk Class III

Registration Details

81040530082

25351266084202045

13179728000174

Company Information

South Korea
PT: CORÉIA DO SUL

Dates and Status

Jan 11, 2021

11/01/2031

09/18/2025 19:00:01