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"Abbot" multiplex collection kit (unsterilized) - Taiwan Registration d627bfb08519a186d31716337130ebd9

Access comprehensive regulatory information for "Abbot" multiplex collection kit (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d627bfb08519a186d31716337130ebd9 and manufactured by ABBOTT MOLECULAR INC.. The authorized representative in Taiwan is ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.).

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d627bfb08519a186d31716337130ebd9
Registration Details
Taiwan FDA Registration: d627bfb08519a186d31716337130ebd9
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Device Details

"Abbot" multiplex collection kit (unsterilized)
TW: "ไบžๅŸน" ๅคš้‡ๆชข้ซ”ๆ”ถ้›†ๅฅ—็ต„ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

d627bfb08519a186d31716337130ebd9

DHA09402158202

Company Information

Product Details

Limited to the classification and grading management measures for medical equipment "Microbial Sample Collection and Delivery Equipment (C.2900)" the first level identification range.

C Immunology and microbiology

C.2900 Microbial sample collection and delivery equipment

Input;; QMS/QSD

Dates and Status

May 27, 2020

May 27, 2030