Taiwan FDA registration f3bf2c7e30ee34450d87af9c0f949df8
"Youkang" High Pressure Liquid Chromatography (Unsterilized)
TW: “佑康” 高壓液相層析儀 (未滅菌)
Registration details
- Analysis ID
- f3bf2c7e30ee34450d87af9c0f949df8
- Customs Code
- DHA04401235303
Company information
- Manufacturer Country
- United States
- Authorized Representative
- PROGRESSIVE GROUP INC.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "High-pressure Liquid Chromatography for Clinical Use (A.2260)".
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.2260 High-pressure liquid chromatography for clinical use
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Nov 09, 2012
- Expiry Date
- Nov 09, 2017
- Cancellation Date
- Nov 21, 2019
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Youkang" High Pressure Liquid Chromatography (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f3bf2c7e30ee34450d87af9c0f949df8 and manufactured by Trinity Biotech (Primus Corporation dba Trinity Biotech). The authorized representative in Taiwan is PROGRESSIVE GROUP INC..
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