Taiwan FDA registration f9c9c11310bb3e089b5acb9828971168

"Abbott" Designer Automated Immunoassay Analyzer (Unsterilized)

TW: "亞培" 設計師自動免疫分析儀 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·FLEXTRONICS MANUFACTURING (SINGAPORE) PTE LTD·Registered Apr 15, 2016 – Apr 15, 2026Cancelled
Registration details
Analysis ID
f9c9c11310bb3e089b5acb9828971168
Customs Code
DHA09401639901
Company information
Manufacturer Country
Singapore
Product details
Intended Use
Limited to the first level identification range of the "Individual Photometric Chemical Analyzer for Clinical Use (A.2160)" of the Measures for the Administration of Medical Devices.
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A.2160 Individual Photometric Chemistry Analyzer for Clinical Use
Import Information
QMS/QSD;; 輸入
Dates and status
Registration Date
Apr 15, 2016
Expiry Date
Apr 15, 2026
Cancellation Date
Sep 30, 2021
Cancellation information
Status
Logged out
Reason
轉為登錄字號
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About this record

Access comprehensive regulatory information for "Abbott" Designer Automated Immunoassay Analyzer (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f9c9c11310bb3e089b5acb9828971168 and manufactured by FLEXTRONICS MANUFACTURING (SINGAPORE) PTE LTD. The authorized representative in Taiwan is ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.).

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including FLEXTRONICS MANUFACTURING (SINGAPORE) PTE LTD, ABBOTT LABORATORIES, and 5 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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