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

Probes - ANVISA Registration 81440809003

Access comprehensive regulatory information for Probes in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81440809003 and manufactured by HANGZHOU FUSHAN MEDICAL APPLIANCES CO.,LTD.. The registration is held by JMM PAULA GARCIA DISTRIBUIDORA ME 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 WELL LEAD MEDICAL CO, LTD, FRESENIUS KABI AG, 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
81440809003
Registration Details
ANVISA Registration Number: 81440809003
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

KIT BioTube-PEG® (PULL) LUXURY
Risk Class II

Registration Details

81440809003

25351076269202141

20740314000138

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Feb 25, 2021

VIGENTE

09/18/2025 19:00:01