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

Connectors - ANVISA Registration 80279429014

Access comprehensive regulatory information for Connectors in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80279429014 and manufactured by BEIJING LEPU MEDICAL TECHNOLOGY CO., LTD.. The registration is held by FORMED - COMERCIO DE PRODUTOS MEDICOS E COSMETICOS 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 BMR MEDICAL S.A., SHANGHAI HEALTH MEDICAL 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
80279429014
Registration Details
ANVISA Registration Number: 80279429014
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

Angioway Manifold
Risk Class II

Registration Details

80279429014

25351393055202489

07139218000170

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Sep 02, 2024

VIGENTE

09/18/2025 19:00:01