Guide Wire - ANVISA Registration 10407999007

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 10407999007 and manufactured by SHUNMEI MEDICAL CO., LTD. The registration is held by ANGIOMED IMPORTACAO E EXPORTACAO 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 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
10407999007
Registration Details
ANVISA Registration Number: 10407999007
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

Shun Skyline - Guia de Troca para Angioplastia PTFE
Risk Class II

Registration Details

10407999007

25351536426202342

02699256000164

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Aug 28, 2023

VIGENTE

09/18/2025 19:00:01