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

Materials for Occlusion Verification - ANVISA Registration 10347940194

Access comprehensive regulatory information for Materials for Occlusion Verification in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 10347940194 and manufactured by PARKELL INC.. The registration is held by WILCOS DO BRASIL INDÚSTRIA E COMÉRCIO 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 DR. JEAN BAUSCH GMBH & CO. KG, FREUDENBERG MEDICAL, LLC, 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
10347940194
Registration Details
ANVISA Registration Number: 10347940194
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

Registration Details

10347940194

25351701652202319

01074837000148

Company Information

PARKELL INC.
United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Oct 30, 2023

VIGENTE

09/18/2025 19:00:01