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Ultrasound-guided peripheral nerve block cannula - ANVISA Registration 82209529224

Access comprehensive regulatory information for Ultrasound-guided peripheral nerve block cannula in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 82209529224 and manufactured by MARDEN MEDICAL LTDA. The registration is held by MARDEN MEDICAL LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including euro parts brasil industria e comercio de instrumental cirurgico ltda, EVEREAST MEDICAL PRODUCTS GROUP 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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82209529224
Registration Details
ANVISA Registration Number: 82209529224
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Device Details

Cânula Híbrida Teflonada Sonovisivel com injetor de Fármaco MedView
Risk Class II

Registration Details

82209529224

25351700687202322

40220751000138

Company Information

Brazil
PT: BRASIL

Dates and Status

Nov 20, 2023

VIGENTE

09/18/2025 19:00:01