Taiwan FDA registration 7d811c076a45f10023500062fe36b1b9
Kunxia protein correction solution
TW: 昆喜亞蛋白質校正液
Taiwan·Risk Class 2·BIOKIT S.A.·Registered Feb 17, 2020 – Feb 17, 2030ActiveRegistration details
- Analysis ID
- 7d811c076a45f10023500062fe36b1b9
- Customs Code
- DHA05603327502
Company information
- Manufacturer
- BIOKIT S.A.
- Manufacturer Country
- Spain
- Authorized Representative
- ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.)
Product details
- Intended Use
- This product is used for the calibration of the analysis of Kunsiya (APET α-1-acid glycoprotein reagent, Kunsiya α-1-antitrypsin test set) by turbidimetric method.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1150 Calibrated Products
- Import Information
- import
Dates and status
- Registration Date
- Feb 17, 2020
- Expiry Date
- Feb 17, 2030
About this record
Access comprehensive regulatory information for Kunxia protein correction solution in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7d811c076a45f10023500062fe36b1b9 and manufactured by BIOKIT S.A.. The authorized representative in Taiwan is ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.).
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