Visit us at Medica, Dusseldorf, Germany 17-20 November 2025 at Hall 16, Stand D17-5 and ask us about our free AI tools and the document builder.
Pure Global

Ureteroscope - ANVISA Registration 80475519056

Access comprehensive regulatory information for Ureteroscope in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80475519056 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 companies making the same product including E-MED PRODUTOS MÉDICO-HOSPITALARES LTDA - ME, SHENZHEN HUGEMED MEDICAL TECHNICAL DEVELOPMENT CO., LTD., 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.

Free Database
Powered by Pure Global AI
100,000+ Devices
5 Competitors
5 Recent Registrations
80475519056
Registration Details
ANVISA Registration Number: 80475519056
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

Ureteroscópio Flexvision Chroma S
Risk Class II

Registration Details

80475519056

25351140164202586

03480968000150

Company Information

Brazil
PT: BRASIL

Dates and Status

Sep 15, 2025

VIGENTE

09/18/2025 19:00:01