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Abboteite test group - Taiwan Registration d314a02523c01ce63c07d2caab0f816e

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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d314a02523c01ce63c07d2caab0f816e
Registration Details
Taiwan FDA Registration: d314a02523c01ce63c07d2caab0f816e
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Device Details

Abboteite test group
TW: ไบžๅŸน็šฎ่„‚้…ฎๆชข้ฉ—่ฉฆๅŠ‘็ต„
Risk Class 2

Registration Details

d314a02523c01ce63c07d2caab0f816e

DHA05603181903

Product Details

This product is a chemiluminescent microparticle immunoassay that quantifies human serum, plasma or urine cortisol on an Alinity i analyzer.

A Clinical chemistry and clinical toxicology

A.1205 Cortisol (hydronephrine, and hydroxycortisol) test system

import

Dates and Status

Dec 05, 2018

Dec 05, 2028