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Abbott Instant Quantitative Polymerase Chain Reaction Analyzer - Taiwan Registration 21db52662aa69cc911770ebd3343b26c

Access comprehensive regulatory information for Abbott Instant Quantitative Polymerase Chain Reaction Analyzer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 21db52662aa69cc911770ebd3343b26c 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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21db52662aa69cc911770ebd3343b26c
Registration Details
Taiwan FDA Registration: 21db52662aa69cc911770ebd3343b26c
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Device Details

Abbott Instant Quantitative Polymerase Chain Reaction Analyzer
TW: ไบžๅŸนๅณๆ™‚ๅฎš้‡่šๅˆ้…ถ้€ฃ้Ž–ๅๆ‡‰ๅˆ†ๆžๅ„€
Risk Class 2

Registration Details

21db52662aa69cc911770ebd3343b26c

DHA05603419404

Company Information

Product Details

This product is an automated system for quantitative and qualitative detection of nucleic acid sequences by fluorescence-based PCR during nucleic acid detection. It is used for nucleic acid detection in clinical laboratories, and the test is jointly completed by Abbott m2000sp automatic specimen processing system (Abbott m2000sp instrument) and this product (Abbott m2000rt instrument).

A Clinical chemistry and clinical toxicology

A.2570 Clinical Multi-standard Detection System Instrument

Input;; QMS/QSD

Dates and Status

Jan 15, 2021

Jan 15, 2026