Taiwan FDA registration 609a085d806fd930694c331ded51da11
"Acerys" Angel platelet thick fluid separation system
TW: “艾思瑞斯” 安杰爾血小板濃厚液分離系統
Taiwan·Risk Class 2·Arthrex, Inc.·Registered Apr 08, 2020 – Apr 08, 2030ActiveRegistration details
- Analysis ID
- 609a085d806fd930694c331ded51da11
- Customs Code
- DHA05603346504
Company information
- Manufacturer
- Arthrex, Inc.
- Manufacturer Country
- United States
- Authorized Representative
- JOINSMART BIOMEDICAL COMPANY LIMITED
Product details
- Intended Use
- This product is used in clinical laboratories or surgical point-of-care to prepare low-concentration platelet plasma and high-concentration platelet plasma from a small amount of whole blood samples or blood bone marrow mixtures of patients.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.9245 Automated hemocytoseparator
- Import Information
- import
Dates and status
- Registration Date
- Apr 08, 2020
- Expiry Date
- Apr 08, 2030
About this record
Access comprehensive regulatory information for "Acerys" Angel 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 609a085d806fd930694c331ded51da11 and manufactured by Arthrex, Inc.. The authorized representative in Taiwan is JOINSMART BIOMEDICAL COMPANY LIMITED.
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