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"Ikfurt" lactic acid tester (unsterilized) - Taiwan Registration c99e36f11829622ebc5aa29c752f7564

Access comprehensive regulatory information for "Ikfurt" lactic acid tester (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c99e36f11829622ebc5aa29c752f7564 and manufactured by EKF-diagnostic GmbH. The authorized representative in Taiwan is SHANG LI INSTRUMENTS CO., LTD..

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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c99e36f11829622ebc5aa29c752f7564
Registration Details
Taiwan FDA Registration: c99e36f11829622ebc5aa29c752f7564
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Device Details

"Ikfurt" lactic acid tester (unsterilized)
TW: โ€œ็›Šๅ…‹็ฆโ€ ไนณ้…ธๆชขๆธฌๅ„€(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

c99e36f11829622ebc5aa29c752f7564

DHA09402179503

Company Information

Germany

Product Details

Limited to the classification and grading management method of medical equipment, lactic acid test system (A.1450) first level identification range.

A Clinical chemistry and clinical toxicology

A.1450 Lactate test system

Input;; QMS/QSD

Dates and Status

Jul 29, 2020

Jul 29, 2025