Taiwan FDA registration 18b48e2cf7cf1975f1215efb1e2c5f45
Dragon K in vitro reagent card
TW: 龍騰K他命體外試劑卡
Taiwan·Risk Class 2·The first factory of Longteng Biotechnology Co., Ltd·Registered Oct 01, 2007 – Oct 01, 2017CancelledRegistration details
- Analysis ID
- 18b48e2cf7cf1975f1215efb1e2c5f45
- Customs Code
- DHY00500246602
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- The first factory of Longteng Biotechnology Co., Ltd
Product details
- Intended Use
- 定性檢測人尿液中的K-他命及其代謝產物(閾值100 ng/mL).
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.0001 苯環利定試驗系統
- Import Information
- Domestic
Dates and status
- Registration Date
- Oct 01, 2007
- Expiry Date
- Oct 01, 2017
- 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 Dragon K in vitro reagent card in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 18b48e2cf7cf1975f1215efb1e2c5f45 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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