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Fujifilm-Determination of blood creatine phosphokinase dry test piece - Taiwan Registration a341bb77e51a5e6dbb1b5d8bf685f09e

Access comprehensive regulatory information for Fujifilm-Determination of blood creatine phosphokinase dry test piece in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a341bb77e51a5e6dbb1b5d8bf685f09e and manufactured by FUJIFILM Healthcare Manufacturing Corporation Minamiashigara Nakanuma Office. The authorized representative in Taiwan is HUNG CHONG CORP..

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a341bb77e51a5e6dbb1b5d8bf685f09e
Registration Details
Taiwan FDA Registration: a341bb77e51a5e6dbb1b5d8bf685f09e
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Device Details

Fujifilm-Determination of blood creatine phosphokinase dry test piece
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Risk Class 2

Registration Details

a341bb77e51a5e6dbb1b5d8bf685f09e

DHA00601583605

Product Details

Measure the concentration of creatine phosphokinase in plasma or serum.

A Clinical chemistry and clinical toxicology

A.1215 Creatine phosphokinase/creatine kinase or isoenzyme testing system

import

Dates and Status

Jan 05, 2006

Jan 05, 2026