Taiwan FDA registration 22e3ecdfcf709a6bf01f6b8f6232cad2
Lingyue-specific immunoglobulin E immunofluorescence detection kit
TW: 凌越特異性免疫球蛋白E免疫螢光檢測試劑套組
Taiwan·Risk Class 2·Lingyue Biomedical Co., Ltd. Taipei Factory·Registered Sep 10, 2012 – Sep 10, 2027ActiveRegistration details
- Analysis ID
- 22e3ecdfcf709a6bf01f6b8f6232cad2
Company information
- Manufacturer
- Lingyue Biomedical Co., Ltd. Taipei Factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Lingyue Biomedical Co., Ltd. Taipei Factory
Product details
- Intended Use
- This product is used for clinical in vitro semi-quantitative analysis of specific immunoglobulin E (specific IgE) content in human serum.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.5510 免疫球蛋白A,G,M,D及E免疫試驗系統
- Import Information
- Domestic
Dates and status
- Registration Date
- Sep 10, 2012
- Expiry Date
- Sep 10, 2027
About this record
Access comprehensive regulatory information for Lingyue-specific immunoglobulin E immunofluorescence detection kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 22e3ecdfcf709a6bf01f6b8f6232cad2 and manufactured by Lingyue Biomedical Co., Ltd. Taipei Factory. The authorized representative in Taiwan is Lingyue Biomedical Co., Ltd. Taipei Factory.
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