“Dio” Hybrid Link - Taiwan Registration dd89ebee90f7c4e2e03fcca32df13432

Access comprehensive regulatory information for “Dio” Hybrid Link in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number dd89ebee90f7c4e2e03fcca32df13432 and manufactured by DIO CORPORATION. The authorized representative in Taiwan is DIO IMPLANT TAIWAN CORPORATION.

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.