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

Colposcope - ANVISA Registration 81504799103

Access comprehensive regulatory information for Colposcope in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81504799103 and manufactured by DYSIS MEDICAL LTD. The registration is held by PASSROD IMPORTAÇÃO E EXPORTAÇÃO DE PRODUTOS PARA SAÚDE LTDA - ME 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 KOLPLAST CI LTDA, GG INDUSTRIA DE EQUIPAMENTOS MEDICOS 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
81504799103
Registration Details
ANVISA Registration Number: 81504799103
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

COLPOSCÓPIO DIGITAL DYSIS
Risk Class II

Registration Details

81504799103

25351298225202331

26185222000110

Company Information

DYSIS MEDICAL LTD
United Kingdom
PT: REINO UNIDO

Dates and Status

May 29, 2023

VIGENTE

09/18/2025 19:00:01