Taiwan FDA registration 52c696ac403a7839df5598238aaf35c1
"Hades" platelet thick fluid separation system
TW: “黑帝斯” 血小板濃厚液分離系統
Taiwan·Risk Class 2·ANDREAS HETTICH GMBH & CO. KG·Registered Jun 10, 2019 – Jun 10, 2029ActiveRegistration details
- Analysis ID
- 52c696ac403a7839df5598238aaf35c1
- Customs Code
- DHA05603244608
Company information
- Manufacturer
- ANDREAS HETTICH GMBH & CO. KG
- Manufacturer Country
- Germany
- Authorized Representative
- JOINSMART BIOMEDICAL COMPANY LIMITED
Product details
- Intended Use
- 本產品搭配Arthrex Double Syringe使用,可從血液樣本中分離出血小板濃厚液.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.9245 Automated hemocytoseparator
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Jun 10, 2019
- Expiry Date
- Jun 10, 2029
About this record
Access comprehensive regulatory information for "Hades" platelet thick fluid separation system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 52c696ac403a7839df5598238aaf35c1 and manufactured by ANDREAS HETTICH GMBH & CO. KG. The authorized representative in Taiwan is JOINSMART BIOMEDICAL COMPANY LIMITED.
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