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Beckman Coulter Arthurs C-peptide correction solution - Taiwan Registration 9ccee79750b6bbada42cd3a847668314

Access comprehensive regulatory information for Beckman Coulter Arthurs C-peptide correction solution in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9ccee79750b6bbada42cd3a847668314 and manufactured by BECKMAN COULTER LABORATORY SYSTEMS (SUZHOU) CO., LTD.;; BECKMAN COULTER INC.. The authorized representative in Taiwan is BECKMAN COULTER TAIWAN INC., TAIWAN BRANCH (U.S.A.).

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9ccee79750b6bbada42cd3a847668314
Registration Details
Taiwan FDA Registration: 9ccee79750b6bbada42cd3a847668314
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Device Details

Beckman Coulter Arthurs C-peptide correction solution
TW: ่ฒๅ…‹ๆ›ผๅบซ็ˆพ็‰นไบž็‘Ÿๆ–ฏC-่ƒœ่‚ฝๆ กๆญฃๆถฒ
Risk Class 2

Registration Details

9ccee79750b6bbada42cd3a847668314

DHA09200128201

Product Details

This product is used to correct Access C-peptide detection, and with the Access immunoassay system, quantitatively determine the concentration of C-peptide in human serum, plasma and urine.

A Clinical chemistry and clinical toxicology

A.1150 Calibrated Products

Input;; QMS/QSD;; Contract manufacturing;; Chinese goods

Dates and Status

Nov 09, 2021

Nov 09, 2026