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

Solution For Ophthalmic Use - ANVISA Registration 80021290015

Access comprehensive regulatory information for Solution For Ophthalmic Use in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80021290015 and manufactured by CRISTÁLIA PRODUTOS QUÍMICOS FARMACÊUTICOS LTDA.. The registration is held by CRISTÁLIA PRODUTOS QUÍMICOS FARMACÊUTICOS LTDA. with validity until Feb 07, 2032.

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including ALCON LABORATORIES, INC, LEBON PRODUTOS QUÍMICOS E FARMACÊUTICOS 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
80021290015
Registration Details
ANVISA Registration Number: 80021290015
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

LUNERA (carmelose sodica 0,5% + glicerol 0,9%) solução oftálmica
Risk Class III

Registration Details

80021290015

25351300046202118

44734671000151

Company Information

Brazil
PT: BRASIL

Dates and Status

Feb 07, 2022

07/02/2032

09/18/2025 19:00:01