“Hospitech”AG Cuffill - Taiwan Registration 47f93007e0b800613fce43979a3c57c9
Access comprehensive regulatory information for “Hospitech”AG Cuffill in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 47f93007e0b800613fce43979a3c57c9 and manufactured by Quasar Electronics Technology (Dongguan) Co., Ltd.;;Hospitech Respiration Ltd.. The authorized representative in Taiwan is TAIWAN MEDICAL SERVICES 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.
Device Details
Registration Details
47f93007e0b800613fce43979a3c57c9
Ministry of Health Medical Device Land Transport No. 001331
DHA09200133101
Product Details
Details are as detailed as approved Chinese instructions
D Anesthesiology
D5750 Inflatable inner tube balloon
Imported from abroad; Contract manufacturing;; Made in China
Dates and Status
Apr 22, 2022
Apr 22, 2027

