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

VEIN VIEWING DEVICE - ANVISA Registration 80213739012

Access comprehensive regulatory information for VEIN VIEWING DEVICE in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80213739012 and manufactured by FABINJECT INDUSTRIA PLASTICA LTDA. The registration is held by FABINJECT INDÚSTRIA E COMÉRCIO IMPORTAÇÃO E EXPORTAÇÃO 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 MEDCAPTAIN MEDICAL TECHNOLOGY CO. LTD., NOVADAQ TECHNOLOGIES ULC, 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
80213739012
Registration Details
ANVISA Registration Number: 80213739012
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

Registration Details

80213739012

25351105805201704

02289126000153

Company Information

Dates and Status

May 08, 2017

VIGENTE

09/18/2025 19:00:01