Guide Wire - ANVISA Registration 81040530065

Access comprehensive regulatory information for Guide Wire in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81040530065 and manufactured by MTW ENDOSCOPIE. The registration is held by PROSURGERY- IMPORTAÇÃO E COMÉRCIO DE MATERIAL CIRÚRGICO 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, SP MEDICAL A/S, 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
81040530065
Registration Details
ANVISA Registration Number: 81040530065
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

FIO GUIA MTW
Risk Class II

Registration Details

81040530065

25351597426201932

13179728000174

Company Information

MTW ENDOSCOPIE
Germany
PT: ALEMANHA

Dates and Status

Nov 18, 2019

VIGENTE

09/18/2025 19:00:01