Visit us at Medica, Dusseldorf, Germany 17-20 November 2025 at Hall 16, Stand D17-5 and ask us about our free AI tools and the document builder.
Pure Global

Catheters - ANVISA Registration 80312270040

Access comprehensive regulatory information for Catheters in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80312270040 and manufactured by TELEFLEX MEDICAL EUROPE LIMITED. The registration is held by TELEFLEX MEDICAL BRASIL LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including COOK INCORPORATED, BOSTON SCIENTIFIC CORPORATION, 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 Competitors
5 Recent Registrations
80312270040
Registration Details
ANVISA Registration Number: 80312270040
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

Cateter Intermitente Liquick X-Treme
Risk Class I

Registration Details

80312270040

25351459814202483

06089071000199

Company Information

Ireland
PT: IRLANDA

Dates and Status

Jan 13, 2025

VIGENTE

09/18/2025 19:00:01