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Abbott designer corticosterone test panel - Taiwan Registration ea009e71ff5d00b95ba0f8e6c9d76c1b

Access comprehensive regulatory information for Abbott designer corticosterone 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 ea009e71ff5d00b95ba0f8e6c9d76c1b 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.).

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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ea009e71ff5d00b95ba0f8e6c9d76c1b
Registration Details
Taiwan FDA Registration: ea009e71ff5d00b95ba0f8e6c9d76c1b
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Device Details

Abbott designer corticosterone test panel
TW: ไบžๅŸน่จญ่จˆๅธซ็šฎ่ณช้…ฎๆชข้ฉ—่ฉฆๅŠ‘็ต„
Risk Class 2

Registration Details

ea009e71ff5d00b95ba0f8e6c9d76c1b

DHA00602000001

Product Details

This product is used for the quantitative detection of corticosterone (cortisol) in human serum, plasma, or urine by chemical cold light microparticle immunoassay (CMIA) on the ARCHITECT i system.

A Clinical chemistry and clinical toxicology

A.1205 ็šฎ่ณช้†‡(ๆฐซๅŸบ่…ŽไธŠ่…บ็ด ,ๅŠ็พฅ็šฎ่ณชๅ›บ้†‡)่ฉฆ้ฉ—็ณป็ตฑ;; A.1150 ๆ กๆญฃๅ“

Contract manufacturing;; input

Dates and Status

Apr 30, 2009

Apr 30, 2029