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

Kit for venous/arterial catheter - ANVISA Registration 80216150002

Access comprehensive regulatory information for Kit for venous/arterial catheter in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80216150002 and manufactured by LIDCO LTD. The registration is held by BRAGENIX LTDA EPP 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 HEALTH QUALITY - INDUSTRIA E COMERCIO LTDA, SHAOXING HAITECH MEDICAL PRODUCTS CO.,LTD, 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
80216150002
Registration Details
ANVISA Registration Number: 80216150002
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

KIT DE INJECAO LIDCO CM 50
Risk Class II

Registration Details

80216150002

25351279866200424

02057708000104

Company Information

LIDCO LTD
United Kingdom
PT: REINO UNIDO

Dates and Status

Apr 29, 2005

VIGENTE

09/18/2025 19:00:01