Taiwan FDA registration fc422584ac97fe817554ea238f891f1f
“Estar” Tropocells PRP Device
TW: “益思達” 妥倍適自體高濃度血小板血漿製備組
Taiwan·Risk Class 2·MD·Estar Technologies Ltd.·Registered Apr 20, 2017 – Apr 20, 2027ActiveRegistration details
- Analysis ID
- fc422584ac97fe817554ea238f891f1f
- License Form
- Ministry of Health Medical Device Import No. 029546
- Customs Code
- DHA05602954602
Company information
- Manufacturer
- Estar Technologies Ltd.
- Manufacturer Country
- Israel
- Authorized Representative
- SYNERGY BIOMEDICAL LTD.
Product details
- Intended Use
- This product is a vacuum blood collection tube containing separating gum for the preparation of high concentration platelets. For ease of operation prior to orthopedic surgery, autologous or allogeneic graft bone can be mixed.
- 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
- Apr 20, 2017
- Expiry Date
- Apr 20, 2027
About this record
Access comprehensive regulatory information for “Estar” Tropocells PRP Device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fc422584ac97fe817554ea238f891f1f and manufactured by Estar Technologies Ltd.. The authorized representative in Taiwan is SYNERGY BIOMEDICAL LTD..
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