Lumbar decompression kit - ANVISA Registration 82209520032

Access comprehensive regulatory information for Lumbar decompression kit in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 82209520032 and manufactured by MARDEN MEDICAL LTDA. The registration is held by MARDEN MEDICAL LTDA with validity until Mar 05, 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 SURGITEC COMERCIO E FABRICAÇÃO DE PRODUTOS MEDICOS E HOSPITALARES LTDA - ME, MARDEN MEDICAL LTDA, 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
82209520032
Registration Details
ANVISA Registration Number: 82209520032
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 Cânula EndoGuide +
Risk Class III

Registration Details

82209520032

25351459061202414

40220751000138

Company Information

Brazil
PT: BRASIL

Dates and Status

Mar 05, 2025

05/03/2035

09/18/2025 19:00:01