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Abbott Designer Cytokeratin 21-1 Test Reagent Set - Taiwan Registration ba23e048b67eb31c20ebbd515c085f16

Access comprehensive regulatory information for Abbott Designer Cytokeratin 21-1 Test Reagent Set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ba23e048b67eb31c20ebbd515c085f16 and manufactured by FUJIREBIO DIAGNOSTICS, INC.;; ABBOTT GMBH. 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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ba23e048b67eb31c20ebbd515c085f16
Registration Details
Taiwan FDA Registration: ba23e048b67eb31c20ebbd515c085f16
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Device Details

Abbott Designer Cytokeratin 21-1 Test Reagent Set
TW: ไบžๅŸน่จญ่จˆๅธซ็ดฐ่ƒž่ง’่ณช่›‹็™ฝ21-1ๆชข้ฉ—่ฉฆๅŠ‘็ต„
Risk Class 2

Registration Details

ba23e048b67eb31c20ebbd515c085f16

DHA00602270000

Company Information

Product Details

This product was used to quantitatively detect human cytokeratin 19 fragments in human serum and plasma by chemical cold light particle immunoassay (CMIA).

C Immunology and microbiology

C.6010 ่…ซ็˜ค็›ธ้—œๆŠ—ๅŽŸๅ…็–ซ่ฉฆ้ฉ—็ณป็ตฑ

Input;; Contract manufacturing

Dates and Status

Aug 12, 2011

Aug 12, 2026