INTRACRANIAL STENT - ANVISA Registration 81836600008

Access comprehensive regulatory information for INTRACRANIAL STENT in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 81836600008 and manufactured by PHENOX GMBH. The registration is held by PHENOX DO BRASIL COMERCIO DE MATERIAS MEDICOS LTDA with validity until May 12, 2035.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including BALT EXTRUSION SAS, Stryker Neurovascular, 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
81836600008
2 Related Devices
Registration Details
ANVISA Registration Number: 81836600008
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

Related Devices (2)

Stent Diversor de Fluxo p64 MW HPC
Risk Class IV

Registration Details

81836600008

25351955328202491

33038158000100

Company Information

PHENOX GMBH
Germany
PT: ALEMANHA

Dates and Status

May 12, 2025

12/05/2035

09/18/2025 19:00:01

Stent Diversor de Fluxo p64 MW HPC
Risk Class IV

Registration Details

81836600008

25351955328202491

33038158000100

Company Information

Dates and Status

May 12, 2025

12/05/2035

09/18/2025 19:00:01