Taiwan FDA registration b022370e962ba19b123583783c6e1b62
"Arkra" magnesium test strip (unsterilized)
TW: "愛科來" 鎂檢測試紙(未滅菌)
Taiwan·Risk Class 1·ARKRAY Factory, Inc., Head office factory·Registered Jan 31, 2023 – Jan 31, 2028ActiveRegistration details
- Analysis ID
- b022370e962ba19b123583783c6e1b62
- Customs Code
- DHA09402302503
Company information
- Manufacturer
- ARKRAY Factory, Inc., Head office factory
- Manufacturer Country
- Japan
- Authorized Representative
- SYNGEN BIOTECH CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the classification and grading management measures for medical equipment "Magnesium Test System (A.1495)".
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1495 Magnesium testing system
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Jan 31, 2023
- Expiry Date
- Jan 31, 2028
About this record
Access comprehensive regulatory information for "Arkra" magnesium test strip (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b022370e962ba19b123583783c6e1b62 and manufactured by ARKRAY Factory, Inc., Head office factory. The authorized representative in Taiwan is SYNGEN BIOTECH CO., LTD..
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