Esophageal Dilators - ANVISA Registration 10334789008

Access comprehensive regulatory information for Esophageal Dilators in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 10334789008 and manufactured by DIVERSATEK HEALTHCARE INC.. The registration is held by G.F.E. DO BRASIL LTDA. with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including JIANGSU VEDKANG MEDICAL SCIENCE AND TECHNOLOGY CO., LTD, DIVERSATEK HEALTHCARE INC., 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
10334789008
Registration Details
ANVISA Registration Number: 10334789008
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

Device Details

BUGIA DILATADORA - M-FLEX
Risk Class I

Registration Details

10334789008

25351263601202458

55126981000100

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

May 20, 2024

VIGENTE

09/18/2025 19:00:01