Nasal Dilator - ANVISA Registration 80245210322

Access comprehensive regulatory information for Nasal Dilator in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80245210322 and manufactured by PHARMAPLAST S.A.E. The registration is held by CREMER 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 ZHEJIANG BANGLI MEDICAL PRODUCTS CO.,LTD., MERIL LIFE SCIENCES PVT LTD, 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.