Flexible Endoscope - ANVISA Registration 10317490122
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 10317490122 and manufactured by FUJIFILM CORPORATION. The registration is held by LABOR MED APARELHAGEM DE PRECISAO LTDA with validity until currently active (VIGENTE).
This page provides complete technical specifications for 2 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.

Janaina dos Santos de Miranda
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Contact Pure Global Brazil TeamRelated Devices (2)
Registration Details
10317490122
25351020451201274
32150633000172
Company Information
Dates and Status
Jul 09, 2012
VIGENTE
09/18/2025 19:00:01
Registration Details
10317490122
25351020451201274
32150633000172
Company Information
Dates and Status
Jul 09, 2012
VIGENTE
09/18/2025 19:00:01
Flexible Endoscope
VIDEOENDOSCĂPIO SĂRIE 600
FUJIFILM OPTICS CO., LTD (MITO)
10317490149
Jul 21, 2014
Flexible Endoscope
VIDEOENDOSCĂPIO SĂRIE 600
FUJIFILM TECHNO PRODUCTS CO LTD.
10317490149
Jul 21, 2014
Flexible Endoscope
VIDEOENDOSCĂPIO SĂRIE 600
FUJIFILM CORPORATION
10317490149
Jul 21, 2014
Flexible Endoscope
VIDEOENDOSCĂPIO
FUJIFILM CORPORATION
10317490214
Oct 31, 2017
Flexible Endoscope
VIDEOENDOSCĂPIO
Not specified
10317499005
Nov 11, 2021
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