Instrumentation For Endoscopy - ANVISA Registration 80475510229

Access comprehensive regulatory information for Instrumentation For Endoscopy in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80475510229 and manufactured by E-MED PRODUTOS MÉDICO-HOSPITALARES LTDA - ME. The registration is held by E-MED PRODUTOS MÉDICO-HOSPITALARES LTDA - ME 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 E-MED PRODUTOS MÉDICO-HOSPITALARES LTDA - ME, GETSCH UND HILLER MEDIZINTECHNIK GMBH, 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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80475510229
Registration Details
ANVISA Registration Number: 80475510229
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Device Details

Endoscópio Rígido E-MED Plus
Risk Class II

Registration Details

80475510229

25351481539201917

03480968000150

Company Information

Brazil
PT: BRASIL

Dates and Status

Sep 09, 2019

VIGENTE

09/18/2025 19:00:01