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Endoscopy Snares - ANVISA Registration 81040530047

Access comprehensive regulatory information for Endoscopy Snares in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81040530047 and manufactured by MEDITALIA S.A.S. The registration is held by PROSURGERY- IMPORTAÇÃO E COMÉRCIO DE MATERIAL CIRÚRGICO LTDA ME with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 1 companies making the same product including United States Endoscopy Group, Inc. (US Endoscopy), and 1 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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81040530047
Registration Details
ANVISA Registration Number: 81040530047
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Device Details

Netis - Alça de Remoção de corpo estranho e pólipos
Risk Class II

Registration Details

81040530047

25351487331201910

13179728000174

Company Information

MEDITALIA S.A.S
Italy
PT: ITÁLIA

Dates and Status

Oct 14, 2019

VIGENTE

09/18/2025 19:00:01

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