“RegenLab” RegenACR-C Plus Type I - Taiwan Registration 8a35080d17aee66ebc23032c448230af

Access comprehensive regulatory information for “RegenLab” RegenACR-C Plus Type I in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8a35080d17aee66ebc23032c448230af and manufactured by REGEN LAB SA. The authorized representative in Taiwan is QUALTECH CONSULTING 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.