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

Applicators - ANVISA Registration 80856010003

Access comprehensive regulatory information for Applicators in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80856010003 and manufactured by SINOLINKS MEDICAL INNOVATION, INC.. The registration is held by agmashi comercio de material medico e serviços de cobranças ltda epp 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 FAGA MEDICAL INDUSTRIA DE EQUIPAMENTOS E INSTRUMENTOS MEDICO-HOSPITALARES LTDA ME, Baxter Healthcare S.A., 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
80856010003
Registration Details
ANVISA Registration Number: 80856010003
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

Dispositivo Removedor descartável - Grampeador de pele (DSSA / DSSB) - Sinolinks Medical
Risk Class I

Registration Details

80856010003

25351308373202452

08234423000188

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Jun 17, 2024

VIGENTE

09/18/2025 19:00:01