Taiwan FDA registration 38b47a1bc80ebeeef8f81b2e22e59e4c

"Beckman Coulter" Arthurs Immunoassay (Unsterilized)

TW: "貝克曼庫爾特"亞瑟斯免疫分析儀 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·BECKMAN COULTER, INC.·Registered Jun 28, 2012 – Jun 28, 2022Cancelled
Registration details
Analysis ID
38b47a1bc80ebeeef8f81b2e22e59e4c
Customs Code
DHA04401189600
Company information
Manufacturer Country
United States
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
Input;; QMS/QSD
Dates and status
Registration Date
Jun 28, 2012
Expiry Date
Jun 28, 2022
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 "Beckman Coulter" Arthurs Immunoassay (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 38b47a1bc80ebeeef8f81b2e22e59e4c and manufactured by BECKMAN COULTER, INC.. The authorized representative in Taiwan is BECKMAN COULTER TAIWAN INC., TAIWAN BRANCH (U.S.A.).

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including BECKMAN COULTER, INC., and 1 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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