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“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.

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47f93007e0b800613fce43979a3c57c9
Registration Details
Taiwan FDA Registration: 47f93007e0b800613fce43979a3c57c9
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Device Details

“Hospitech”AG Cuffill
TW: “霍比特”氣囊壓力控制器
Risk Class 2
MD

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