Flexible Endoscope - ANVISA Registration 80011680013

Access comprehensive regulatory information for Flexible Endoscope in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80011680013 and manufactured by HOYA CORPORATION. The registration is held by WELCH ALLYN DO BRASIL, COMÉRCIO DE EQUIPAMENTOS MÉDICOS 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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80011680013
Registration Details
ANVISA Registration Number: 80011680013
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Device Details

FIBROCOLONOSCOPIO PENTAX
Risk Class I

Registration Details

80011680013

25351014486200365

03135603000199

Company Information

HOYA CORPORATION
Japan
PT: JAPÃO

Dates and Status

Feb 18, 2004

VIGENTE

09/18/2025 19:00:01