"Termao" single use of guide wire - Taiwan Registration 3740f5388cd8b0947c5c9e31c70c1277

Access comprehensive regulatory information for "Termao" single use of guide wire in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3740f5388cd8b0947c5c9e31c70c1277 and manufactured by (O) TERUMO CORPORATION;;( P)TERUMO CORPORATION ASHITAKA FACTORY. The authorized representative in Taiwan is YUAN LI INSTRUMENT CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including TERUMO CORPORATION;; ASHITAKA FACTORY OF TERUMO CORPORATION, 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.