INTRACRANIAL STENT - ANVISA Registration 80005430444
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 80005430444 and manufactured by Stryker Neurovascular. The registration is held by STRYKER DO BRASIL LTDA with validity until Nov 21, 2026.
This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including BALT EXTRUSION SAS, PHENOX GMBH, 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.
Related Devices (2)
Registration Details
80005430444
25351384999201657
02966317000102
Company Information
Dates and Status
Nov 21, 2016
21/11/2026
09/18/2025 19:00:01
STENT INTRACRANIANO
Stent Diversor de Fluxo p48 MW
PHENOX GMBH
81836600009
Jul 14, 2025
STENT INTRACRANIANO
Stent Diversor de Fluxo p48 MW
Not specified
81836600009
Jul 14, 2025
STENT INTRACRANIANO
Stent Diversor de Fluxo p64 MW HPC
PHENOX GMBH
81836600008
May 12, 2025
STENT INTRACRANIANO
Stent Diversor de Fluxo p64 MW HPC
Not specified
81836600008
May 12, 2025
STENT INTRACRANIANO
Stent Diversor de Fluxo p64 MW
PHENOX GMBH
81836600006
Feb 03, 2025

