Taiwan FDA registration 59061eaad0a66bcc9c7f5830873c4f74

"Sysmecon" automatic blood coagulation analyzer

TW: “希森美康”全自動血液凝固分析儀
Taiwan flagTaiwan·Risk Class 2·SYSMEX CORPORATION; SYSMEX RA CO., LTD.·Registered May 28, 2013 – May 28, 2028Active
Registration details
Analysis ID
59061eaad0a66bcc9c7f5830873c4f74
Customs Code
DHA00602470109
Company information
Manufacturer Country
Japan
Authorized Representative
SYSMEX TAIWAN CO., LTD.
Product details
Intended Use
This device is an in vitro diagnostic automatic blood coagulation analyzer for blood coagulation testing in clinical laboratories.
Product Type (Level 1)
B Hematology, pathology, and genetics
Product Type (Level 2)
B.5400 Agglomer
Import Information
import
Dates and status
Registration Date
May 28, 2013
Expiry Date
May 28, 2028
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About this record

Access comprehensive regulatory information for "Sysmecon" automatic blood coagulation analyzer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 59061eaad0a66bcc9c7f5830873c4f74 and manufactured by SYSMEX CORPORATION; SYSMEX RA CO., LTD.. The authorized representative in Taiwan is SYSMEX TAIWAN CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 3 companies making similar products including SYSMEX CORPORATION;; SYSMEX CORPORATION, I-SQUARE, SYSMEX CORPORATION, I-SQUARE, and 5 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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