Taiwan FDA registration 82bca15d93da2cf5881246611341eeff
“Terumo” SmartPReP2 Centrifuge System
TW: “泰爾茂” 斯麥特離心系統
Taiwan·Risk Class 2·MD·TERUMO BCT, INC.·Registered Jul 11, 2016 – Jul 11, 2021ExpiredRegistration details
- Analysis ID
- 82bca15d93da2cf5881246611341eeff
- License Form
- Ministry of Health Medical Device Import No. 028455
- Customs Code
- DHA05602845507
Company information
- Manufacturer
- TERUMO BCT, INC.
- Manufacturer Country
- United States
- Authorized Representative
- TERUMO TAIWAN MEDICAL CO., LTD.
Product details
- Intended Use
- This product needs to be used with the "Termao" Smet Platelet Rich Plasma Treatment Kit, which uses a small amount of blood samples from patients to separate platelet thick fluid.
- Product Type (Level 1)
- B Hematology and pathology devices
- Product Type (Level 2)
- B9245 Automatic Hematology Cell Separator
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 11, 2016
- Expiry Date
- Jul 11, 2021
About this record
Access comprehensive regulatory information for “Terumo” SmartPReP2 Centrifuge System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 82bca15d93da2cf5881246611341eeff and manufactured by TERUMO BCT, INC.. The authorized representative in Taiwan is TERUMO TAIWAN MEDICAL CO., LTD..
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.
Free DatabasePowered by Pure Global AI89,000+ Devices