Taiwan FDA registration c15b33c68c384381643bc68d0a7b6428
Pukasa Biotech K Tama Test Reagent
TW: 璞笠生技K他命檢驗試劑
Taiwan·Risk Class 2·PULI BIOTECHNOLOGY CO., LTD.·Registered Dec 22, 2022 – Dec 22, 2027ActiveRegistration details
- Analysis ID
- c15b33c68c384381643bc68d0a7b6428
Company information
- Manufacturer
- PULI BIOTECHNOLOGY CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- PULI BIOTECHNOLOGY CO., LTD.
Product details
- Intended Use
- This product uses qualitative detection of the concentration of KET in human urine, and the threshold standard of this product for KET is set to 100ng/ml. Can be used by professionals and general staff.
- 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
- QMS/QSD;; 國產
Dates and status
- Registration Date
- Dec 22, 2022
- Expiry Date
- Dec 22, 2027
About this record
Access comprehensive regulatory information for Pukasa Biotech K Tama Test Reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c15b33c68c384381643bc68d0a7b6428 and manufactured by PULI BIOTECHNOLOGY CO., LTD.. The authorized representative in Taiwan is PULI BIOTECHNOLOGY CO., LTD..
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