Taiwan FDA registration b49fc0ad6db26c63c9df1a7e668da7ea

Abbott integrated chip technology serological correction solution

TW: 亞培整合晶片技術血清校正液組
Taiwan flagTaiwan·Risk Class 2·FISHER DIAGNOSTICS, A DIVISION OF FISHER SCIENTIFIC COMPANY, LLC, A PART OF THERMO FISHER SCIENTIFIC INC.;; ABBOTT GMBH·Registered Jan 11, 2019 – Jan 11, 2029Active
Registration details
Analysis ID
b49fc0ad6db26c63c9df1a7e668da7ea
Customs Code
DHA05603211205
Company information
Manufacturer Country
United States;;Germany
Product details
Intended Use
The product is used for the correction of sodium, potassium and chlorine analysis in serum and needs to be used with the Alinity ci system.
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 11, 2019
Expiry Date
Jan 11, 2029
About this record

Access comprehensive regulatory information for Abbott integrated chip technology serological 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 b49fc0ad6db26c63c9df1a7e668da7ea and manufactured by FISHER DIAGNOSTICS, A DIVISION OF FISHER SCIENTIFIC COMPANY, LLC, A PART OF THERMO FISHER SCIENTIFIC INC.;; ABBOTT GMBH. The authorized representative in Taiwan is ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.).

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