Taiwan FDA registration f4f482011ff4c68131d99bcaf0c4649d
Abbott second-generation urea nitrogen assay set
TW: 亞培第二代尿素氮檢驗試劑組
Taiwan·Risk Class 2·ABBOTT IRELAND DIAGNOSTICS DIVISION·Registered Dec 13, 2021 – Dec 13, 2026ActiveRegistration details
- Analysis ID
- f4f482011ff4c68131d99bcaf0c4649d
- Customs Code
- DHA05603492109
Company information
- Manufacturer
- ABBOTT IRELAND DIAGNOSTICS DIVISION
- Manufacturer Country
- Ireland
- Authorized Representative
- ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.)
Product details
- Intended Use
- This product is used to quantify urea nitrogen in human serum, plasma or urine on the Alinity c System.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1770 尿素氮試驗系統
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Dec 13, 2021
- Expiry Date
- Dec 13, 2026
About this record
Access comprehensive regulatory information for Abbott second-generation urea nitrogen assay set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f4f482011ff4c68131d99bcaf0c4649d and manufactured by ABBOTT IRELAND DIAGNOSTICS DIVISION. The authorized representative in Taiwan is ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.).
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