"Termao" Ge Lai guide the set - Taiwan Registration 086558ac5b463d50d8ddaf11d50e5021

Access comprehensive regulatory information for "Termao" Ge Lai guide the set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 086558ac5b463d50d8ddaf11d50e5021 and manufactured by TERUMO CORPORATION;; ASHITAKA FACTORY OF TERUMO CORPORATION. The authorized representative in Taiwan is TERUMO TAIWAN MEDICAL CO., 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.