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 80218010040

Access comprehensive regulatory information for Instrument Kit in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80218010040 and manufactured by GS MEDICAL CO LTD. The registration is held by ORTOMEDIC DISTRIBUIDORA DE PRODUTOS MEDICOS 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
80218010040
Registration Details
ANVISA Registration Number: 80218010040
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

Instrumental para Cage AnyPlus PLIF
Risk Class I

Registration Details

80218010040

25351485713201603

65564536000185

Company Information

GS MEDICAL CO LTD
South Korea
PT: CORร‰IA DO SUL

Dates and Status

Dec 26, 2016

VIGENTE

09/18/2025 19:00:01