Cimosir D Gemini High Sensitivity Tube Solution - Taiwan Registration 365d171d4aed677981e9ae3c32ecdfe3

Access comprehensive regulatory information for Cimosir D Gemini High Sensitivity Tube Solution in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 365d171d4aed677981e9ae3c32ecdfe3 and manufactured by INSTRUMENTATION LABORATORY CO.;; BIOKIT S.A.. The authorized representative in Taiwan is Werfen Taiwan Limited.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including INSTRUMENTATION LABORATORY CO.;; BIOKIT S.A., and 1 recent registrations in the same category. 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.