Puncture Assistance Kit - ANVISA Registration 10237610248

Access comprehensive regulatory information for Puncture Assistance Kit in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 10237610248 and manufactured by KOLPLAST CI LTDA. The registration is held by KOLPLAST CI LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search, 3 companies making the same product including KOLPLAST CI LTDA, MEDTRONIC, INC., and 3 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.