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

Gel - ANVISA Registration 81963410001

Access comprehensive regulatory information for Gel in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 81963410001 and manufactured by HONY MEDICAL CO., LTD.. The registration is held by GENESYSMED BRASIL 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 RMC - INDÚSTRIA BRASILEIRA DE PRODUTOS MÉDICOS LTDA, HELIANTO FARMACEUTICA LTDA, 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
81963410001
Registration Details
ANVISA Registration Number: 81963410001
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

KIT ESTÉRIL PARA ULTRASSOM
Risk Class I

Registration Details

81963410001

25351224261202440

33412395000199

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

May 13, 2024

VIGENTE

09/18/2025 19:00:01