Flexible Endoscope - ANVISA Registration 10317490149

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 10317490149 and manufactured by FUJIFILM TECHNO PRODUCTS CO LTD.. The registration is held by LABOR MED APARELHAGEM DE PRECISAO LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for 3 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search, 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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10317490149
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Registration Details
ANVISA Registration Number: 10317490149
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Risk Class II

Registration Details

10317490149

25351644373201395

32150633000172

Company Information

Japan
PT: JAPÃO

Dates and Status

Jul 21, 2014

VIGENTE

09/18/2025 19:00:01

VIDEOENDOSCÓPIO SÉRIE 600
Risk Class II

Registration Details

10317490149

25351644373201395

32150633000172

Company Information

Japan
PT: JAPÃO

Dates and Status

Jul 21, 2014

VIGENTE

09/18/2025 19:00:01

VIDEOENDOSCÓPIO SÉRIE 600
Risk Class II

Registration Details

10317490149

25351644373201395

32150633000172

Company Information

Japan
PT: JAPÃO

Dates and Status

Jul 21, 2014

VIGENTE

09/18/2025 19:00:01