Flexible Endoscope - ANVISA Registration 10317490148

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 10317490148 and manufactured by FUJIFILM OPTICS CO., LTD (MITO). 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.

Free Database
Powered by Pure Global AI
100,000+ Devices
5 Similar Products
5 Competitors
10317490148
3 Related Devices
Registration Details
ANVISA Registration Number: 10317490148
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

🇧🇷 Brazil Regulatory Expert

Need help with your Brazil registration?

Contact Pure Global Brazil Team
Free consultation

Related Devices (3)

ENTEROSCÓPIO EN-580T
Risk Class II

Registration Details

10317490148

25351608479201300

32150633000172

Company Information

Japan
PT: JAPÃO

Dates and Status

Jul 14, 2014

VIGENTE

09/18/2025 19:00:01

ENTEROSCÓPIO EN-580T
Risk Class II

Registration Details

10317490148

25351608479201300

32150633000172

Company Information

Japan
PT: JAPÃO

Dates and Status

Jul 14, 2014

VIGENTE

09/18/2025 19:00:01

ENTEROSCÓPIO EN-580T
Risk Class II

Registration Details

10317490148

25351608479201300

32150633000172

Company Information

Japan
PT: JAPÃO

Dates and Status

Jul 14, 2014

VIGENTE

09/18/2025 19:00:01