NordiFlex PenMate - Taiwan Registration 09ef46011535c80cf90c3bf717150009

Access comprehensive regulatory information for NordiFlex PenMate in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 09ef46011535c80cf90c3bf717150009 and manufactured by Novo Nordisk A/S. The authorized representative in Taiwan is NOVO NORDISK PHARMA (TAIWAN) LTD..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.