Endoscopic electrosurgical electrode, bipolar, single use - ANVISA Registration 82209520056

Access comprehensive regulatory information for Endoscopic electrosurgical electrode, bipolar, single use in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 82209520056 and manufactured by MARDEN MEDICAL LTDA. The registration is held by MARDEN MEDICAL LTDA with validity until May 26, 2035.

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 MARDEN MEDICAL LTDA, E-MED PRODUTOS MÉDICO-HOSPITALARES LTDA - ME, 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
82209520056
Registration Details
ANVISA Registration Number: 82209520056
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

Kit Canula para Anuloplastia percutânea Dirigível Orthoplus +
Risk Class III

Registration Details

82209520056

25351018156202554

40220751000138

Company Information

Brazil
PT: BRASIL

Dates and Status

May 26, 2025

26/05/2035

09/18/2025 19:00:01