Taiwan FDA registration 32c249456630dc16ff2ab80e69d0f69d
“SEAWON” Autologous Platelet Rich Plasma Kit
TW: “希旺” 血小板濃厚液自動分離組
Taiwan·Risk Class 2·MD·Seawon Meditech Co., Ltd.·Registered Jan 16, 2017 – Jan 16, 2022ExpiredRegistration details
- Analysis ID
- 32c249456630dc16ff2ab80e69d0f69d
- License Form
- Ministry of Health Medical Device Import No. 029191
- Customs Code
- DHA05602919104
Company information
- Manufacturer
- Seawon Meditech Co., Ltd.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- SINCERE BIOTECH CO., LTD.
Product details
- Intended Use
- This product isolates platelet thick fluid from blood samples and is used in mixed bone surgery for autologous and allogeneic grafts.
- 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
- Jan 16, 2017
- Expiry Date
- Jan 16, 2022
About this record
Access comprehensive regulatory information for “SEAWON” Autologous Platelet Rich Plasma Kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 32c249456630dc16ff2ab80e69d0f69d and manufactured by Seawon Meditech Co., Ltd.. The authorized representative in Taiwan is SINCERE BIOTECH CO., LTD..
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