Taiwan FDA registration e78e276b77cb4979ea57b779e69685ed

"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 CORPORATION, I-SQUARE·Registered May 26, 2017 – May 26, 2027Active
Registration details
Analysis ID
e78e276b77cb4979ea57b779e69685ed
Customs Code
DHA05602956802
Company information
Manufacturer Country
Japan
Authorized Representative
SYSMEX TAIWAN CO., LTD.
Product details
Intended Use
This product is a fully automatic blood coagulation analyzer, in vitro diagnosis is used in clinical chemistry laboratories to analyze blood coagulation, colorization, immunoanalysis and agglutination methods.
Product Type (Level 1)
B Hematology, pathology, and genetics
Product Type (Level 2)
B.5425 Versatile system for in vitro agglutination studies
Import Information
import
Dates and status
Registration Date
May 26, 2017
Expiry Date
May 26, 2027
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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 e78e276b77cb4979ea57b779e69685ed and manufactured by SYSMEX CORPORATION;; SYSMEX CORPORATION, I-SQUARE. The authorized representative in Taiwan is SYSMEX TAIWAN CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 4 companies making similar products including SYSMEX CORPORATION, I-SQUARE, SYSMEX CORPORATION;; 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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