Taiwan FDA registration 8b1097e3828330afb208bd5458a73054
Kunxia immunoglobulin test set
TW: 昆喜亞免疫球蛋白檢驗試劑組
Taiwan·Risk Class 2·BIOKIT, S.A.·Registered Jan 30, 2012 – Jan 30, 2027ActiveRegistration details
- Analysis ID
- 8b1097e3828330afb208bd5458a73054
- Customs Code
- DHA00602309600
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 with the ARCHITECT c system to quantitatively test immunoglobulin E (IgE) in human serum or plasma.
- 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
- Jan 30, 2012
- Expiry Date
- Jan 30, 2027
About this record
Access comprehensive regulatory information for Kunxia immunoglobulin test set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8b1097e3828330afb208bd5458a73054 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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