Taiwan FDA registration d314a02523c01ce63c07d2caab0f816e

Abboteite test group

TW: 亞培皮脂酮檢驗試劑組
Taiwan flagTaiwan·Risk Class 2·FISHER DIAGNOSTICS, A DIVISION OF FISHER SCIENTIFIC COMPANY, LLC, A PART OF THERMO FISHER SCIENTIFIC INC.;; ABBOTT IRELAND DIAGNOSTICS DIVISION·Registered Dec 05, 2018 – Dec 05, 2028Active
Registration details
Analysis ID
d314a02523c01ce63c07d2caab0f816e
Customs Code
DHA05603181903
Company information
Manufacturer Country
Ireland;;United States
Product details
Intended Use
This product is a chemiluminescent microparticle immunoassay that quantifies human serum, plasma or urine cortisol on an Alinity i analyzer.
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A.1205 Cortisol (hydronephrine, and hydroxycortisol) test system
Import Information
import
Dates and status
Registration Date
Dec 05, 2018
Expiry Date
Dec 05, 2028
About this record

Access comprehensive regulatory information for Abboteite test group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d314a02523c01ce63c07d2caab0f816e and manufactured by FISHER DIAGNOSTICS, A DIVISION OF FISHER SCIENTIFIC COMPANY, LLC, A PART OF THERMO FISHER SCIENTIFIC INC.;; ABBOTT IRELAND DIAGNOSTICS DIVISION. The authorized representative in Taiwan is ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.).

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