Taiwan FDA registration bc184aced35979837bb6ac0aa31ae08b

"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 Kakogawa Factory·Registered Mar 24, 2016 – Mar 24, 2026Expired
Registration details
Analysis ID
bc184aced35979837bb6ac0aa31ae08b
Customs Code
DHA05602831402
Company information
Manufacturer Country
Japan
Authorized Representative
SYSMEX TAIWAN CO., LTD.
Product details
Intended Use
This instrument is an in vitro diagnostic analyzer for sampling and analyzing human blood plasma components with anticoagulant (sodium citrate). Fibrin differentiation (FDP) analysis can be performed using plasma and serological samples.
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
Mar 24, 2016
Expiry Date
Mar 24, 2026
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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 bc184aced35979837bb6ac0aa31ae08b and manufactured by SYSMEX CORPORATION;; SYSMEX CORPORATION Kakogawa Factory. 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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