Taiwan FDA registration b6ec539d1291b2142d5d8c641165e139
“Arthrex” Angel Blood Processing Set
TW: “艾思瑞斯” 安杰爾血液分離套組
Taiwan·Risk Class 2·MD·Arthrex, Inc.·Registered Jul 22, 2020 – Jul 22, 2025ExpiredRegistration details
- Analysis ID
- b6ec539d1291b2142d5d8c641165e139
- License Form
- Ministry of Health Medical Device Import No. 033510
- Customs Code
- DHAS5603351004
Company information
- Manufacturer
- Arthrex, Inc.
- Manufacturer Country
- United States
- Authorized Representative
- JOINSMART BIOMEDICAL COMPANY LIMITED
Product details
- Intended Use
- This product must be equipped with the "Aceres" Angel platelet thick fluid separation system for the concentration of high-concentration platelet plasma from whole blood or blood bone marrow fluid.
- 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
- Jul 22, 2020
- Expiry Date
- Jul 22, 2025
About this record
Access comprehensive regulatory information for “Arthrex” Angel Blood Processing Set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b6ec539d1291b2142d5d8c641165e139 and manufactured by Arthrex, Inc.. The authorized representative in Taiwan is JOINSMART BIOMEDICAL COMPANY LIMITED.
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