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Flexible Endoscope - ANVISA Registration 81769779005

Access comprehensive regulatory information for Flexible Endoscope in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81769779005 and manufactured by SHENZHEN HUGEMED TECHNICAL DEVELOPMENT CO. LTD. ( MAWU ROAD). The registration is held by ENDO MED PRODUTOS MEDICOS 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 FUJIFILM CORPORATION, OLYMPUS MEDICAL SYSTEMS CORP., 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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81769779005
Registration Details
ANVISA Registration Number: 81769779005
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Device Details

ENDOSCÓPIO Flexível HUGEMED SeeScope HU
Risk Class II

Registration Details

81769779005

25351370077202471

29397137000103

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Aug 26, 2024

VIGENTE

09/18/2025 19:00:01