Sigmoidoscope - ANVISA Registration 10317490220
Access comprehensive regulatory information for Sigmoidoscope in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10317490220 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 this device, regulatory compliance details, 5 similar products found using AI-powered semantic search. 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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Registration Details
10317490220
25351472005201908
32150633000172
Company Information
Dates and Status
Sep 09, 2019
VIGENTE
09/18/2025 19:00:01
Flexible Endoscope
VIDEOENDOSC脫PIO S脡RIE 720
FUJIFILM CORPORATION
10317490221
Oct 07, 2019
Flexible Endoscope
ENDOSCOPIO VIDEOCOLONOSCOPIO VIDEOSIGMOIDOSCOPIO
OLYMPUS MEDICAL SYSTEMS CORP.
80124630026
Oct 15, 2003
Gastroduodenoscope
VIDEOENDOSC脫PIO S脡RIE 760
FUJIFILM CORPORATION
10317490216
Dec 11, 2017
Flexible Endoscope
VIDEOENDOSC脫PIO S脡RIE 400/500
FUJIFILM CORPORATION
10317490122
Jul 09, 2012
Flexible Endoscope
VIDEOENDOSC脫PIO S脡RIE 400/500
FUJINON SINGAPORE PTE. LTD.
10317490122
Jul 09, 2012