Taiwan FDA registration 708cd002db45e444fc2a5fb51c1eef10
Shiji 1502 electrophoresis test kit
TW: 世基1502電泳檢測套組
Taiwan·Risk Class 2·Shiji Biomedical Co., Ltd. Taipei Plant·Registered Feb 05, 2010 – Feb 05, 2025ExpiredRegistration details
- Analysis ID
- 708cd002db45e444fc2a5fb51c1eef10
- Customs Code
- DHY00500302602
Company information
- Manufacturer
- Shiji Biomedical Co., Ltd. Taipei Plant
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- PHARMIGENE, INC.
Product details
- Intended Use
- The Shiji 1502 electrophoresis test set was used to qualitatively detect HLA-B*1502 gene by polymerase chain reaction technology.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.3360 Genotype testing system for drug metabolic enzymes
- Import Information
- Domestic
Dates and status
- Registration Date
- Feb 05, 2010
- Expiry Date
- Feb 05, 2025
About this record
Access comprehensive regulatory information for Shiji 1502 electrophoresis test kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 708cd002db45e444fc2a5fb51c1eef10 and manufactured by Shiji Biomedical Co., Ltd. Taipei Plant. The authorized representative in Taiwan is PHARMIGENE, INC..
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