Taiwan FDA registration 7876ccf43c3dbc3a343ff2284fdaa3bd
"AGL" lactic acid detector (unsterilized)
TW: "愛科來" 乳酸檢測儀 (未滅菌)
Taiwan·Risk Class 1·ARKRAY Factory, Inc.,Head office factory·Registered Dec 23, 2015 – Dec 23, 2025ExpiredRegistration details
- Analysis ID
- 7876ccf43c3dbc3a343ff2284fdaa3bd
- Customs Code
- DHA09401600802
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 classification and grading management method of medical equipment, lactic acid test system (A.1450) first level identification range.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1450 Lactate test system
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Dec 23, 2015
- Expiry Date
- Dec 23, 2025
About this record
Access comprehensive regulatory information for "AGL" lactic acid detector (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 7876ccf43c3dbc3a343ff2284fdaa3bd and manufactured by ARKRAY Factory, Inc.,Head office factory. The authorized representative in Taiwan is SYNGEN BIOTECH CO., LTD..
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