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

Cannulas - ANVISA Registration 80047300472

Access comprehensive regulatory information for Cannulas in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80047300472 and manufactured by DUCTH OPHTHALMIC RESEARCH CENTER INTERNATIONAL BV. The registration is held by MEDSTAR IMPORTAÇÃO E EXPORTAÇÃO 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 TRACOE MEDICAL GMBH, MARDEN MEDICAL 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
80047300472
Registration Details
ANVISA Registration Number: 80047300472
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

CÂNULA OFTÁLMICA PARA IRRIGAÇÃO E ASPIRAÇÃO, USO ÚNICO DORC
Risk Class II

Registration Details

80047300472

25351394864201299

03580620000135

Company Information

Netherlands
PT: HOLANDA (PAÍSES BAIXOS)

Dates and Status

May 27, 2013

VIGENTE

09/18/2025 19:00:01