Catheter Insertion Kit - ANVISA Registration 80081350392

Access comprehensive regulatory information for Catheter Insertion Kit in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80081350392 and manufactured by ARGON MEDICAL DEVICES INC. The registration is held by FLEX LAB COMERCIO DE MATERIAIS CIRURGICOS E HOSPITALARES LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including ARGON MEDICAL DEVICES, INC, APT MEDICAL 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.

Free Database
Powered by Pure Global AI
100,000+ Devices
5 Similar Products
5 Competitors
80081350392
Registration Details
ANVISA Registration Number: 80081350392
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

Device Details

Minikit Cateter Arterial Argon
Risk Class II

Registration Details

80081350392

25351150520201541

02620178000160

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Jul 20, 2015

VIGENTE

09/18/2025 19:00:01