Taiwan FDA registration 22e4d16b83cec67c9fd009415acc2f92
Longteng morphine in vitro reagent card
TW: 龍騰嗎啡體外試劑卡
Taiwan·Risk Class 2·The first factory of Longteng Biotechnology Co., Ltd·Registered Dec 07, 2006 – Dec 07, 2016CancelledRegistration details
- Analysis ID
- 22e4d16b83cec67c9fd009415acc2f92
- Customs Code
- DHY00500229001
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 morphine and its metabolites in human urine.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.3640 嗎啡試驗系統
- 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 morphine 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 22e4d16b83cec67c9fd009415acc2f92 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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