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

Instrument Kit - ANVISA Registration 10444710011

Access comprehensive regulatory information for Instrument Kit in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10444710011 and manufactured by CENTRAL MEDICAL TECHNOLOGIES, INC.. The registration is held by SENDAI ORTOPEDIA IMPORTAÇÃO 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 MARDEN MEDICAL LTDA, LIMA CORPORATE S.P.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
10444710011
Registration Details
ANVISA Registration Number: 10444710011
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

VESSEL-X INSTRUMENTAL PARA CIFOPLASTIA A-SPINE
Risk Class II

Registration Details

10444710011

25351105862201194

00127383000163

Company Information

Taiwan
PT: TAIWAN

Dates and Status

Apr 11, 2011

VIGENTE

09/18/2025 19:00:01