Taiwan FDA registration ce15135bc23af6cac1060f20080b761a
QUANTIA ASO STANDARD
TW: 昆喜亞抗鏈球菌溶血素O檢驗試劑組 標準液
Taiwan·Risk Class 2·MD·BIOKIT S.A.·Registered Jan 09, 2020 – Jan 09, 2025ExpiredRegistration details
- Analysis ID
- ce15135bc23af6cac1060f20080b761a
- License Form
- Ministry of Health Medical Device Import No. 033128
- Customs Code
- DHA05603312802
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 to establish the calibration of the Kunxia antistreptolysin O test set by turbidimetric method.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1150 calibrate
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 09, 2020
- Expiry Date
- Jan 09, 2025
About this record
Access comprehensive regulatory information for QUANTIA ASO STANDARD in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ce15135bc23af6cac1060f20080b761a 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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