Taiwan FDA registration cb7043fc7e94641cfc98ab00dd24850f

Beckman Coulter Arthurs Free Estriol Correction Solution

TW: 貝克曼庫爾特亞瑟斯游離雌三醇校正液

Taiwan·Risk Class 2·BECKMAN COULTER, INC.·Registered Apr 19, 2024 – Apr 19, 2029Active

Registration details

Analysis ID: cb7043fc7e94641cfc98ab00dd24850f
Customs Code: DHA05603707501

Company information

Manufacturer: BECKMAN COULTER, INC.
Manufacturer Country: United States
Authorized Representative: BECKMAN COULTER TAIWAN INC., TAIWAN BRANCH (U.S.A.)

Product details

Intended Use: 本校正液用來校正貝克曼庫爾特亞瑟斯游離雌三醇試劑組(Access Unconjugated Estriol Reagent)檢測,此分析搭配 Access 免疫分析系統定量偵測人類血清中游離雌三醇濃度.
Product Type (Level 1): A Clinical chemistry and clinical toxicology
Product Type (Level 2): A.1150 Calibrated Products
Import Information: Input;; QMS/QSD

Dates and status

Registration Date: Apr 19, 2024
Expiry Date: Apr 19, 2029

About this record

Access comprehensive regulatory information for Beckman Coulter Arthurs Free Estriol 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 cb7043fc7e94641cfc98ab00dd24850f and manufactured by BECKMAN COULTER, INC.. The authorized representative in Taiwan is BECKMAN COULTER TAIWAN INC., TAIWAN BRANCH (U.S.A.).

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