Taiwan FDA registration f722877763c0cbc4229aec5a8bd8ea39

"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 22, 2011 – Apr 22, 2021Cancelled
Registration details
Analysis ID
f722877763c0cbc4229aec5a8bd8ea39
Customs Code
DHA04401025101
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
Contract manufacturing;; input
Dates and status
Registration Date
Apr 22, 2011
Expiry Date
Apr 22, 2021
Cancellation Date
Aug 15, 2023
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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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 f722877763c0cbc4229aec5a8bd8ea39 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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