Taiwan FDA registration d9ee04c7df6d10e7efce65f6f8d78776
Ulex Ovulation Test Card (Unsterilized)
TW: 優來排卵檢測卡(未滅菌)
Registration details
- Analysis ID
- d9ee04c7df6d10e7efce65f6f8d78776
Company information
- Manufacturer
- Longteng Biotechnology Co., Ltd
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- U-LIANG PHARMACEUTICAL CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the "luteinizing hormone test system (A.1485)" of the Measures for the Administration of Medical Equipment.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1485 Progesterone testing system
- Import Information
- Contract manufacturing;; Domestic
Dates and status
- Registration Date
- Mar 26, 2008
- Expiry Date
- Mar 26, 2018
- Cancellation Date
- Nov 17, 2017
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for Ulex Ovulation Test Card (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d9ee04c7df6d10e7efce65f6f8d78776 and manufactured by Longteng Biotechnology Co., Ltd. The authorized representative in Taiwan is U-LIANG PHARMACEUTICAL CO., LTD..
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