Taiwan FDA registration 2322cf631e6de63bc50d002cc02c92cf
"Termao" Spistrong Aputia Collection Line
TW: “泰爾茂” 思倍壯亞普緹亞收集管路
Taiwan·Risk Class 2·TERUMO BCT, INC.;; TFB MANUFACTURING SRL·Registered Apr 14, 2015 – Apr 14, 2030ActiveRegistration details
- Analysis ID
- 2322cf631e6de63bc50d002cc02c92cf
- Customs Code
- DHA05602720709
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
- For details, it is Chinese approved copy of the imitation order
- 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
- import
Dates and status
- Registration Date
- Apr 14, 2015
- Expiry Date
- Apr 14, 2030
About this record
Access comprehensive regulatory information for "Termao" Spistrong Aputia 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 2322cf631e6de63bc50d002cc02c92cf and manufactured by TERUMO BCT, INC.;; TFB MANUFACTURING SRL. The authorized representative in Taiwan is TERUMO TAIWAN MEDICAL CO., LTD..
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