Taiwan FDA registration b6f20df5dc8dd0b5c01acd3346c36507
Qiaolian electrolyte analysis system
TW: 喬聯電解質分析系統
Taiwan·Risk Class 2·Qiaolian Technology Co., Ltd. Nankan Factory·Registered May 28, 2018 – May 28, 2028ActiveRegistration details
- Analysis ID
- b6f20df5dc8dd0b5c01acd3346c36507
Company information
- Manufacturer
- Qiaolian Technology Co., Ltd. Nankan Factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- BIOCARE CORPORATION
Product details
- Intended Use
- This product can quantitatively detect the pH value in human serum and whole blood, as well as the concentration of sodium, potassium, chloride, calcium and other ions, and provide the concentration of neutralizing calcium ions (nCa) by calculation.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1170 氯化物試驗系統;; A.1670 山梨糖去氫酵素試驗系統;; A.1145 鈣試驗系統
- Import Information
- Domestic
Dates and status
- Registration Date
- May 28, 2018
- Expiry Date
- May 28, 2028
About this record
Access comprehensive regulatory information for Qiaolian electrolyte analysis system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b6f20df5dc8dd0b5c01acd3346c36507 and manufactured by Qiaolian Technology Co., Ltd. Nankan Factory. The authorized representative in Taiwan is BIOCARE CORPORATION.
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