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 82195309041

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 82195309041 and manufactured by SHENZHEN MAIWEI BIOTECH CO., LTD.. The registration is held by PURE LATAM BRAZIL COMERCIO DE PRODUTOS HOSPITALARES 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
82195309041
Registration Details
ANVISA Registration Number: 82195309041
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

Tubo Conector de Pressão
Risk Class II

Registration Details

82195309041

25351078328202549

27939884000109

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

May 26, 2025

VIGENTE

09/18/2025 19:00:01