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"Siemens" creatinine reagent - Taiwan Registration d692d7f737f86d2e65a1ead3090f57cf

Access comprehensive regulatory information for "Siemens" creatinine reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d692d7f737f86d2e65a1ead3090f57cf and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS INC.;; RANDOX LABORATORIES LTD.. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including RANDOX LABORATORIES LTD.;; Siemens Healthcare Diagnostics 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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d692d7f737f86d2e65a1ead3090f57cf
Registration Details
Taiwan FDA Registration: d692d7f737f86d2e65a1ead3090f57cf
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Device Details

"Siemens" creatinine reagent
TW: โ€œ่ฅฟ้–€ๅญโ€่‚Œ้…ธ้…่ฉฆๅŠ‘
Risk Class 2

Registration Details

d692d7f737f86d2e65a1ead3090f57cf

DHA00601996204

Company Information

Product Details

Detection of creatinine concentrations in human serum, plasma, and urine.

A Clinical chemistry and clinical toxicology

A.1225 ่‚Œๆฐจ้…ธ้…่ฉฆ้ฉ—็ณป็ตฑ(Creatininetestsystem)

Contract manufacturing;; input

Dates and Status

Mar 11, 2009

Mar 11, 2029

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