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

Extension - ANVISA Registration 80309549002

Access comprehensive regulatory information for Extension in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80309549002 and manufactured by SHANGHAI HEALTH MEDICAL CO., LTD. The registration is held by MEDILAR IMPORTAÇÃO E DISTRIBUIÇÃO DE PRODUTOS MÉDICO HOSPITALARES S/A 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 ICU MEDICAL, INC (SAN CLEMENT), SEROPLAST INDÚSTRIA E COMÉRCIO DE PRODUTOS HOSPITALARES LTDA -ME, 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
80309549002
Registration Details
ANVISA Registration Number: 80309549002
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

extensor de perfusão - isento de dehp
Risk Class II

Registration Details

80309549002

25351378474202229

07752236000123

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Oct 06, 2022

VIGENTE

09/18/2025 19:00:01