Taiwan FDA registration 47f93007e0b800613fce43979a3c57c9
“Hospitech”AG Cuffill
TW: “霍比特”氣囊壓力控制器
Taiwan·Risk Class 2·MD·Quasar Electronics Technology (Dongguan) Co., Ltd.;;Hospitech Respiration Ltd.·Registered Apr 22, 2022 – Apr 22, 2027ActiveRegistration details
- Analysis ID
- 47f93007e0b800613fce43979a3c57c9
- License Form
- Ministry of Health Medical Device Land Transport No. 001331
- Customs Code
- DHA09200133101
Company information
- Manufacturer Country
- China;;Israel
- Authorized Representative
- TAIWAN MEDICAL SERVICES CORPORATION
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D5750 Inflatable inner tube balloon
- Import Information
- Imported from abroad; Contract manufacturing;; Made in China
Dates and status
- Registration Date
- Apr 22, 2022
- Expiry Date
- Apr 22, 2027
About this record
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.
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