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Api myoglobin test set - Taiwan Registration efc182d750cdf2c41ecb01b9ed097f17

Access comprehensive regulatory information for Api myoglobin test set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number efc182d750cdf2c41ecb01b9ed097f17 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.).

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including BIOKIT, S.A., FISHER DIAGNOSTICS, A DIVISION OF FISHER SCIENTIFIC COMPANY, LLC, A PART OF THERMO FISHER SCIENTIFIC INC.;; ABBOTT IRELAND DIAGNOSTICS DIVISION, and 2 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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efc182d750cdf2c41ecb01b9ed097f17
Registration Details
Taiwan FDA Registration: efc182d750cdf2c41ecb01b9ed097f17
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Device Details

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

Registration Details

efc182d750cdf2c41ecb01b9ed097f17

DHA05603350503

Product Details

This product is used to quantitatively detect myoglobin in human serum and plasma by chemical cold light particle immunoassay (CMIA) on the Alinity i analyzer.

C Immunology and microbiology

C.5680 ่‚Œ็ด…่›‹็™ฝๅ…็–ซ่ฉฆ้ฉ—็ณป็ตฑ

Input;; Contract manufacturing

Dates and Status

Jul 14, 2020

Jul 14, 2025