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Api myoglobin test set calibration solution - Taiwan Registration 7040a8ad4568064cfa01bd318c82c9d3

Access comprehensive regulatory information for Api myoglobin test set calibration solution in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7040a8ad4568064cfa01bd318c82c9d3 and manufactured by FISHER DIAGNOSTICS, A DIVISION OF FISHER SCIENTIFIC COMPANY, LLC, A PART OF THERMO FISHER SCIENTIFIC INC.;; ABBOTT IRELAND DIAGNOSTICS DIVISION. The authorized representative in Taiwan is ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.).

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7040a8ad4568064cfa01bd318c82c9d3
Registration Details
Taiwan FDA Registration: 7040a8ad4568064cfa01bd318c82c9d3
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Device Details

Api myoglobin test set calibration solution
TW: ไบžๅŸน่‚Œ็ด…่›‹็™ฝๆชข้ฉ—่ฉฆๅŠ‘็ต„ ๆ กๆญฃๆถฒ
Risk Class 2

Registration Details

7040a8ad4568064cfa01bd318c82c9d3

DHA05603329100

Product Details

This product is used to calibrate the Alinity i analyzer for the quantitative detection of myoglobin in human serum and plasma.

A Clinical chemistry and clinical toxicology

A.1150 Calibrated Products

Input;; Contract manufacturing

Dates and Status

Mar 13, 2020

Mar 13, 2030