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Abbott Designer i Weber Acid Test Set - Taiwan Registration f4c04c301f153dccf31f5d20cc6e85e4

Access comprehensive regulatory information for Abbott Designer i Weber Acid Test Set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f4c04c301f153dccf31f5d20cc6e85e4 and manufactured by DENKA CO., LTD;; 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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f4c04c301f153dccf31f5d20cc6e85e4
Registration Details
Taiwan FDA Registration: f4c04c301f153dccf31f5d20cc6e85e4
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Device Details

Abbott Designer i Weber Acid Test Set
TW: ไบžๅŸน่จญ่จˆๅธซ i ๅ‰ไผฏ็›Š้…ธๆชข้ฉ—่ฉฆๅŠ‘็ต„
Risk Class 2

Registration Details

f4c04c301f153dccf31f5d20cc6e85e4

DHA00602155509

Product Details

This product is used for the quantitative measurement of the antiepileptic drug valproic acid in human serum or plasma by in vitro chemical cold light microparticle immunoassay (CMIA) on the ARCHITECT i system equipped with the STAT program. The measurements obtained are used to monitor the concentration of Waiberic acid to help ensure appropriate treatment.

A Clinical chemistry and clinical toxicology

A.3645 Radioreceptor Analysis Test System for Neuroleptics

import

Dates and Status

Sep 30, 2010

Sep 30, 2025