Taiwan FDA registration 6e2d96ae5bf2072bb0c167a63e71f6e7
Longteng α fetoprotein in vitro reagent card (serum)
TW: 龍騰α胎蛋白體外試劑卡 (血清)
Taiwan·Risk Class 2·The first factory of Longteng Biotechnology Co., Ltd·Registered Dec 07, 2006 – Dec 07, 2016CancelledRegistration details
- Analysis ID
- 6e2d96ae5bf2072bb0c167a63e71f6e7
- Customs Code
- DHY00500229103
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- The first factory of Longteng Biotechnology Co., Ltd
Product details
- Intended Use
- Qualitative detection of AFP in human serum.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.6010 腫瘤相關抗原免疫試驗系統
- Import Information
- Domestic
Dates and status
- Registration Date
- Dec 07, 2006
- Expiry Date
- Dec 07, 2016
- Cancellation Date
- Dec 13, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Longteng α fetoprotein in vitro reagent card (serum) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6e2d96ae5bf2072bb0c167a63e71f6e7 and manufactured by The first factory of Longteng Biotechnology Co., Ltd. The authorized representative in Taiwan is The first factory of Longteng Biotechnology Co., Ltd.
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