INTRACRANIAL STENT - ANVISA Registration 80691600001
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 80691600001 and manufactured by manufacturer not specified. The registration is held by LFD COMMERCE LTDA with validity until Dec 23, 2029.
This page provides complete technical specifications for 2 related devices, regulatory compliance details, 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.
Related Devices (2)
Registration Details
80691600001
25351766483201897
11162204000145
Company Information
Dates and Status
Dec 23, 2019
23/12/2029
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

