Taiwan FDA registration 7b17a0199ef5e4dfb696637dbb489ad6
Mycobacterium tuberculosis asia rapid test kit (unsterilized)
TW: 亞洲基因結核分枝桿菌快速檢驗試劑套組(未滅菌)
Taiwan·Risk Class 1·Asia Genomics Technology Co., Ltd. Factory 1·Registered Jun 03, 2009 – Jun 03, 2024ExpiredRegistration details
- Analysis ID
- 7b17a0199ef5e4dfb696637dbb489ad6
- Customs Code
- DHY04300247507
Company information
- Manufacturer
- Asia Genomics Technology Co., Ltd. Factory 1
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Asia Genomics Technology Co., Ltd. Factory 1
Product details
- Intended Use
- Limited to the classification and grading management method of medical equipment, Mycobacterium tuberculosis immunofluorescent reagent (C.3370) first level identification range.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.3370 結核桿菌免疫螢光試劑
- Import Information
- Domestic
Dates and status
- Registration Date
- Jun 03, 2009
- Expiry Date
- Jun 03, 2024
About this record
Access comprehensive regulatory information for Mycobacterium tuberculosis asia rapid test kit (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 7b17a0199ef5e4dfb696637dbb489ad6 and manufactured by Asia Genomics Technology Co., Ltd. Factory 1. The authorized representative in Taiwan is Asia Genomics Technology Co., Ltd. Factory 1.
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