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"Siemens" San Dino creatine kinase isoenzyme test group - Taiwan Registration 95d4c1a14784575d26d5954a71f9f050

Access comprehensive regulatory information for "Siemens" San Dino creatine kinase isoenzyme test group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 95d4c1a14784575d26d5954a71f9f050 and manufactured by SENTINEL CH. SPA. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.

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95d4c1a14784575d26d5954a71f9f050
Registration Details
Taiwan FDA Registration: 95d4c1a14784575d26d5954a71f9f050
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Device Details

"Siemens" San Dino creatine kinase isoenzyme test group
TW: โ€œ่ฅฟ้–€ๅญโ€ ่–ๅธ่ซพ ่‚Œ้…ธๆฟ€้…ถๅŒๅŠŸ้…ถๆชข้ฉ—่ฉฆๅŠ‘็ต„
Risk Class 2

Registration Details

95d4c1a14784575d26d5954a71f9f050

DHA05603522102

Company Information

Italy

Product Details

This product is used in vitro diagnostics with Atellica CH Analyzer to inhibitively determine creatine kinase isoenzyme activity (CK-MB and CK-BB) in serum and plasma.

A Clinical chemistry and clinical toxicology

A.1215 Skin Acid Acid Acid Intense ้…ถ / Skin Acid Acid Intense ้…ถ ๆˆ–ๅŒๅŠŸ้…ถ่ฉฆ้ฉ—็ณป็ตฑ;; A.1660 Grade Material (Analysis Material Non-Analysis);; A.1150 Calibrated Products

Input;; QMS/QSD

Dates and Status

Feb 21, 2022

Feb 21, 2027