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Prinmos CLC385 fully automated glycoglogen detection kit - Taiwan Registration f3d7c92b90bf912ad1f33309875df7ab

Access comprehensive regulatory information for Prinmos CLC385 fully automated glycoglogen detection kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f3d7c92b90bf912ad1f33309875df7ab and manufactured by Trinity Biotech (Primus Corporation dba Trinity Biotech). The authorized representative in Taiwan is PROGRESSIVE GROUP INC..

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f3d7c92b90bf912ad1f33309875df7ab
Registration Details
Taiwan FDA Registration: f3d7c92b90bf912ad1f33309875df7ab
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Device Details

Prinmos CLC385 fully automated glycoglogen detection kit
TW: ๆ™ฎๆž—่Žซๆ–ฏCLC385ๅ…จ่‡ชๅ‹•ๅŒ–้†ฃๅŒ–่ก€่‰ฒ็ด ๆชขๆธฌ่ฉฆๅŠ‘็ต„
Risk Class 2
Cancelled

Registration Details

f3d7c92b90bf912ad1f33309875df7ab

DHA00601582500

Company Information

Product Details

It is used in the Prinsmuth CLC385 automatic glycosylated hemoglobin analysis system to quantify glycosylated hemoglobin in vitro diagnostic test by high-pressure liquid chromatography in normal or diabetic patients.

B Hematology, pathology, and genetics

B.7470 Analysis of glycosylated hemoglobin

import

Dates and Status

Jan 05, 2006

Jan 05, 2016

May 28, 2018

Cancellation Information

Logged out

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