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ENDOSCOPY SYSTEM - ANVISA Registration 80421079018

Access comprehensive regulatory information for ENDOSCOPY SYSTEM in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80421079018 and manufactured by ZHONGSHAN WESSE MEDITECH CO., LTD.. The registration is held by MEDHCIR MEDICAL TRADING 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 OLYMPUS MEDICAL SYSTEMS CORP., SHANGHAI SEEGEN PHOTOELECTRIC TECHNOLY CO., 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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80421079018
Registration Details
ANVISA Registration Number: 80421079018
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Device Details

Endoscopio Flexivel Digital com Processador de Video Imagem Urolline.
Risk Class II

Registration Details

80421079018

25351903092202165

03383476000147

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Dec 09, 2021

VIGENTE

09/18/2025 19:00:01