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ENDOSCOPY SYSTEM - ANVISA Registration 81595559005

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 81595559005 and manufactured by HUGER MEDICAL INSTRUMENT CO., LTD.. The registration is held by MF MEDICAL - LTDA - ME 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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81595559005
Registration Details
ANVISA Registration Number: 81595559005
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Device Details

SISTEMA DE VÍDEOENDOSCOPIA NEW ARTHIFLEX GASTRODUODENOSCÓPIO
Risk Class II

Registration Details

81595559005

25351398301202227

13520397000194

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Nov 21, 2022

VIGENTE

09/18/2025 19:00:01