Plethysmograph - ANVISA Registration 81408229005

Access comprehensive regulatory information for Plethysmograph in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81408229005 and manufactured by Timpel S.A.. The registration is held by Timpel S.A. 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 TIMPEL S.A., EKOVUK MEDI S.R.O., 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.