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"Abbott" Alinity i 2nd Generation Testosterone Reagent Kit (Non-Sterile) - Taiwan Registration 6c18f5291a10036465cdcb84de03376e

Access comprehensive regulatory information for "Abbott" Alinity i 2nd Generation Testosterone Reagent Kit (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 6c18f5291a10036465cdcb84de03376e and manufactured by Axis-Shield Diagnostics Limited. The authorized representative in Taiwan is ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.).

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6c18f5291a10036465cdcb84de03376e
Registration Details
Taiwan FDA Registration: 6c18f5291a10036465cdcb84de03376e
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Device Details

"Abbott" Alinity i 2nd Generation Testosterone Reagent Kit (Non-Sterile)
TW: "ไบžๅŸน"็ฌฌไบŒไปฃ็ชไธธ่„‚้…ฎ่ฉฆๅŠ‘็ต„(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

6c18f5291a10036465cdcb84de03376e

Ministry of Health Medical Device Import No. 018860

DHA09401886004

Company Information

Product Details

Limited to the first level identification range of the "testicular lipoketone test system (A.1680)" of the Measures for the Administration of Medical Equipment.

A Clinical chemistry and clinical toxicology

A1680 Testicular Lipoketone Test System

Imported from abroad

Dates and Status

Mar 05, 2018

Mar 05, 2028