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“Abbott” A-1-AGP Reagent Kit (Non-Sterile) - Taiwan Registration 7e0b7e39713962ccf0973ab1fd29cb52

Access comprehensive regulatory information for “Abbott” A-1-AGP 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 7e0b7e39713962ccf0973ab1fd29cb52 and manufactured by BIOKIT S.A.. The authorized representative in Taiwan is ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.).

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7e0b7e39713962ccf0973ab1fd29cb52
Registration Details
Taiwan FDA Registration: 7e0b7e39713962ccf0973ab1fd29cb52
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Device Details

“Abbott” A-1-AGP Reagent Kit (Non-Sterile)
TW: “亞培” α-1-酸性醣蛋白試劑 (未滅菌)
Risk Class 1
MD

Registration Details

7e0b7e39713962ccf0973ab1fd29cb52

Ministry of Health Medical Device Import No. 019473

DHA09401947302

Company Information

Product Details

Limited to the first level identification range of the medical device management method α-1-glycoprotein immunoassay system (C.5420).

C Immunology and microbiology devices

C5420 α-1-glycoprotein immunoassay system

Imported from abroad

Dates and Status

Aug 09, 2018

Aug 09, 2028