Taiwan FDA registration 41502f9dcd13bcb14edf3aa44fbc404f

"Sysmecon" automatic blood analyzer

TW: “希森美康” 全自動血液分析儀
Taiwan flagTaiwan·Risk Class 2·SYSMEX CORPORATION, I-SQUARE·Registered Jan 15, 2021 – Jan 15, 2026Expired
Registration details
Analysis ID
41502f9dcd13bcb14edf3aa44fbc404f
Customs Code
DHA05603419200
Company information
Manufacturer Country
Japan
Authorized Representative
SYSMEX TAIWAN CO., LTD.
Product details
Intended Use
This product is an automated blood analyzer for in vitro diagnostics in clinical laboratories. It is only used to measure human blood, body fluids or quality blood.
Product Type (Level 1)
B Hematology, pathology, and genetics
Product Type (Level 2)
B.5220 Automatic Differentiation Cell Counter
Import Information
QMS/QSD;; 輸入
Dates and status
Registration Date
Jan 15, 2021
Expiry Date
Jan 15, 2026
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About this record

Access comprehensive regulatory information for "Sysmecon" automatic blood analyzer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 41502f9dcd13bcb14edf3aa44fbc404f and manufactured by SYSMEX CORPORATION, I-SQUARE. 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, KAKOGAWA FACTORY, SYSMEX CORPORATION;; SYSMEX CORPORATION Kakogawa Factory, and 3 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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