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

Ophthalmologic Unit - ANVISA Registration 81527870001

Access comprehensive regulatory information for Ophthalmologic Unit in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 81527870001 and manufactured by CARL ZEISS MEDITEC AG. The registration is held by CARL ZEISS VISION BRASIL INDUSTRIA OPTICA 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 APRAMED INDUSTRIA E COMERCIO DE APARELHOS MEDICOS LTDA, TOMEY CORPORATION, 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
81527870001
Registration Details
ANVISA Registration Number: 81527870001
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

Foróptero Digital VISUPHOR 500
Risk Class I

Registration Details

81527870001

25351121411202545

28826394000908

Company Information

Germany
PT: ALEMANHA

Dates and Status

Aug 25, 2025

VIGENTE

09/18/2025 19:00:01