SPERM DNA FRAGMENTATION - ANVISA Registration 82100720003

Access comprehensive regulatory information for SPERM DNA FRAGMENTATION in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 82100720003 and manufactured by PECINI INDUSTRIA E COMERCIO DE PLASTICOS EIRELLI. The registration is held by PECINI INDUSTRIA E COMERCIO DE PLASTICOS EIRELLI with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 4 companies making the same product including BIOTECH VISION CARE PVT. LTD, SUPPORT IMPORTACAO, EXPORTACAO E DISTRIBUICAO LTDA, 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.