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Venous Catheter Kit - ANVISA Registration 80102512987

Access comprehensive regulatory information for Venous Catheter Kit in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80102512987 and manufactured by ANGIODYNAMICS, INC. The registration is held by VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDA with validity until Apr 10, 2033.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including BMR MEDICAL S.A., BARD ACCESS SYSTEMS, INC, 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.

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80102512987
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Registration Details
ANVISA Registration Number: 80102512987
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Related Devices (2)

CATETER DE HEMODIÁLISE CRÔNICA DURAMAX – KIT BÁSICO
Risk Class III

Registration Details

80102512987

25351126110202265

04718143000194

Company Information

ANGIODYNAMICS, INC
United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Apr 10, 2023

10/04/2033

09/18/2025 19:00:01

CATETER DE HEMODIÁLISE CRÔNICA DURAMAX – KIT BÁSICO
Risk Class III

Registration Details

80102512987

25351126110202265

04718143000194

Dates and Status

Apr 10, 2023

10/04/2033

09/18/2025 19:00:01