Beam guide catheter for peripheral atherectomy laser system - ANVISA Registration 10256400075
Access comprehensive regulatory information for Beam guide catheter for peripheral atherectomy laser system in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 10256400075 and manufactured by manufacturer not specified. The registration is held by BIOMEDICAL PRODUTOS CIENTIFICOS MEDICOS E HOSPITALARES S A with validity until Dec 28, 2035.
This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search. 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.

Janaina dos Santos de Miranda
🇧🇷 Brazil Regulatory Expert
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Contact Pure Global Brazil TeamRelated Devices (2)
Registration Details
10256400075
25351644440202076
19848316000166
Company Information
Dates and Status
Jul 20, 2020
28/12/2035
09/18/2025 19:00:01
PERIPHERAL ANGIOPLASTY BALLOON CATHETER
SABER PTA Dilatation Catheter
CORDIS CASHEL
81356112290
Aug 14, 2017
PERIPHERAL ANGIOPLASTY BALLOON CATHETER
CATETER DE DILATACAO PARA PTA
CORDIS CASHEL
81576620023
Mar 06, 2023
PERIPHERAL ANGIOPLASTY BALLOON CATHETER
CATETER DE DILATACAO PARA PTA
Not specified
81576620023
Mar 06, 2023
PERIPHERAL ANGIOPLASTY BALLOON CATHETER
CATETER DE DILATACAO PARA PTA
CORDIS EUROPA N.V.
81576620023
Mar 06, 2023
PERIPHERAL ANGIOPLASTY BALLOON CATHETER
Drug Eluting Balloon Catheters
Not specified
81464750096
Aug 23, 2021