Taiwan FDA registration fe27258a597aa4e25fdd5c1e50b81cb8
“Tubex” Super PRP tube system
TW: “默瀚” 保存血小板濃縮液之容器
Taiwan·Risk Class 2·MD·MOOHAN ENTERPRISE CO., LTD.·Registered Nov 03, 2015 – Nov 03, 2025ExpiredRegistration details
- Analysis ID
- fe27258a597aa4e25fdd5c1e50b81cb8
- License Form
- Ministry of Health Medical Device Import No. 027897
- Customs Code
- DHA05602789708
Company information
- Manufacturer
- MOOHAN ENTERPRISE CO., LTD.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- Sung Ann Medical Equipment .LTD
Product details
- Intended Use
- This product is used to preserve blood and platelet concentrate (PRP) after hemocentrifugation, which can be used for autologous and allogeneic bone mixing surgery.
- 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
- Nov 03, 2015
- Expiry Date
- Nov 03, 2025
About this record
Access comprehensive regulatory information for “Tubex” Super PRP tube system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fe27258a597aa4e25fdd5c1e50b81cb8 and manufactured by MOOHAN ENTERPRISE CO., LTD.. The authorized representative in Taiwan is Sung Ann Medical Equipment .LTD.
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