Rectosigmoidoscope - ANVISA Registration 10237610186
Access comprehensive regulatory information for Rectosigmoidoscope in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 10237610186 and manufactured by KOLPLAST CI LTDA. The registration is held by KOLPLAST CI 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, 3 companies making the same product including KOLPLAST CI LTDA, FRADEL-MED IND E COM DE APARELHOS MEDICOS LTDA-ME, and 3 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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Registration Details
10237610186
25351058236201902
59231530000193
Company Information
Dates and Status
Mar 18, 2019
VIGENTE
09/18/2025 19:00:01
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FRADEL-MED IND E COM DE APARELHOS MEDICOS LTDA-ME
80039960023
Mar 30, 2015
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RETOSIGMOIDOSCĂPIO DESCARTĂVEL FERRARI
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10382810054
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Retosigmoidoscopio
RETOSIGMOIDOSCOPIO DESCARTAVEL KOLPLAST
KOLPLAST CI LTDA
10237610002
Dec 07, 1994