Visit us at Medica, Dusseldorf, Germany 17-20 November 2025 at Hall 16, Stand D17-5 and ask us about our free AI tools and the document builder.
Pure Global

ESOPHAGEAL STENT - ANVISA Registration 81040530018

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 81040530018 and manufactured by manufacturer not specified. The registration is held by PROSURGERY- IMPORTAÇÃO E COMÉRCIO DE MATERIAL CIRÚRGICO LTDA ME with validity until Mar 05, 2028.

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.

Free Database
Powered by Pure Global AI
100,000+ Devices
5 Competitors
5 Recent Registrations
81040530018
2 Related Devices
Registration Details
ANVISA Registration Number: 81040530018
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Related Devices (2)

Prótese Esofágica Revestida Niti-S
Risk Class III

Registration Details

81040530018

25351377693201671

13179728000174

Dates and Status

Mar 05, 2018

05/03/2028

09/18/2025 19:00:01

Prótese Esofágica Revestida Niti-S
Risk Class III

Registration Details

81040530018

25351377693201671

13179728000174

Company Information

South Korea
PT: CORÉIA DO SUL

Dates and Status

Mar 05, 2018

05/03/2028

09/18/2025 19:00:01