Flexible Endoscope - ANVISA Registration 80088379007

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 80088379007 and manufactured by MACHIDA ENDOSCOPE CO. LTD.. The registration is held by FERRARI MEDICAL 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, 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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80088379007
Registration Details
ANVISA Registration Number: 80088379007
Janaina dos Santos de Miranda

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Device Details

VĂ­deo Nasofaringo-laringoscĂłpio FlexĂ­vel ENT-30VE
Risk Class II

Registration Details

80088379007

25351199055202222

00593614000124

Company Information

Japan
PT: JAPÃO

Dates and Status

Mar 31, 2022

VIGENTE

09/18/2025 19:00:01