Taiwan FDA registration 0677468741a5155c51ed819eb47c4d5e
"Termao" Spistrong Putia platelet and plasma collection line
TW: "泰爾茂" 思倍壯亞普緹亞血小板及血漿收集管路
Taiwan·Risk Class 2·TERUMO BCT, INC.;; TFB MANUFACTURING SRL·Registered Oct 28, 2020 – Oct 28, 2025ExpiredRegistration details
- Analysis ID
- 0677468741a5155c51ed819eb47c4d5e
- Customs Code
- DHA05603369508
Company information
- Manufacturer
- TERUMO BCT, INC.;; TFB MANUFACTURING SRL
- Manufacturer Country
- Costa Rica;;United States
- Authorized Representative
- TERUMO TAIWAN MEDICAL CO., LTD.
Product details
- Intended Use
- This product is used with the "Termo" Spistrong Aputia blood cell separator and can be used to collect platelets and plasma.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.9100 Containers for the collection and disposal of blood and blood components
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Oct 28, 2020
- Expiry Date
- Oct 28, 2025
About this record
Access comprehensive regulatory information for "Termao" Spistrong Putia platelet and plasma collection line in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0677468741a5155c51ed819eb47c4d5e and manufactured by TERUMO BCT, INC.;; TFB MANUFACTURING SRL. The authorized representative in Taiwan is TERUMO TAIWAN MEDICAL CO., LTD..
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