Taiwan FDA registration d2520056dc66737485b4820c4ce1794e
Abbott digitoxin test panel
TW: 亞培毛地黃毒素檢驗試劑組
Taiwan·Risk Class 2·B.R.A.H.M.S GmbH;; MICROGENICS CORPORATION·Registered Oct 02, 2019 – Oct 02, 2029ActiveRegistration details
- Analysis ID
- d2520056dc66737485b4820c4ce1794e
- Customs Code
- DHA05603293204
Company information
- Manufacturer
- B.R.A.H.M.S GmbH;; MICROGENICS CORPORATION
- Manufacturer Country
- United States;;Germany
- Authorized Representative
- ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.)
Product details
- Intended Use
- This product analysis is used to quantify in vitro measurements of human serum or plasma in foxglove on an Alinity c analyzer.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.3320 毛地黃毒素試驗系統
- Import Information
- Contract manufacturing;; input
Dates and status
- Registration Date
- Oct 02, 2019
- Expiry Date
- Oct 02, 2029
About this record
Access comprehensive regulatory information for Abbott digitoxin test panel in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d2520056dc66737485b4820c4ce1794e and manufactured by B.R.A.H.M.S GmbH;; MICROGENICS CORPORATION. The authorized representative in Taiwan is ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.).
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