Instrumentation For Suture and Suture Removal - ANVISA Registration 10237619029

Access comprehensive regulatory information for Instrumentation For Suture and Suture Removal in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10237619029 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 companies making the same product including APOLLO ENDOSURGERY, INC., MEDICAL ACTION INDUSTRIES INC., 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.