Flexible Endoscope - ANVISA Registration 80329720056

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 80329720056 and manufactured by RUSSER BRASIL LTDA. The registration is held by RUSSER BRASIL 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.

Free Database
Powered by Pure Global AI
100,000+ Devices
5 Similar Products
5 Competitors
80329720056
Registration Details
ANVISA Registration Number: 80329720056
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

🇧🇷 Brazil Regulatory Expert

Need help with your Brazil registration?

Contact Pure Global Brazil Team
Free consultation

Device Details

ENDOSCÓPIO FLEXÍVEL DIGITAL
Risk Class II

Registration Details

80329720056

25351660965202059

05454389000169

Company Information

RUSSER BRASIL LTDA
Brazil
PT: BRASIL

Dates and Status

Aug 24, 2020

VIGENTE

09/18/2025 19:00:01