SPACER - ANVISA Registration 80112550007

Access comprehensive regulatory information for SPACER in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80112550007 and manufactured by NINGBO MFLAB (YINDONG) MEDICAL INSTRUMENTS CO., LTD. The registration is held by NSR INDÚSTRIA, COMÉRCIO E REPRESENTAÇÕES 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 PLASTIC WAY PRODUTOS PARA A SAÚDE LTDA, HUIZHOU KAIYI TECHNOLOGY CO.,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.