Taiwan FDA registration 07eb66dbddfcf36ec7a952519e49a762

"Sysmecon" automatic blood analyzer

TW: “希森美康” 全自動血液分析儀
Taiwan flagTaiwan·Risk Class 2·SYSMEX CORPORATION;; SYSMEX CORPORATION Kakogawa Factory·Registered May 08, 2023 – May 08, 2028Active
Registration details
Analysis ID
07eb66dbddfcf36ec7a952519e49a762
Customs Code
DHA05603617204
Company information
Manufacturer Country
Japan
Authorized Representative
SYSMEX TAIWAN CO., LTD.
Product details
Intended Use
This product is a multi-item automated blood analyzer that classifies and quantifies parameters in whole blood to help diagnose patients in clinical laboratories.
Product Type (Level 1)
B Hematology, pathology, and genetics
Product Type (Level 2)
B.5200 Automated Cell Counter
Import Information
Input;; QMS/QSD
Dates and status
Registration Date
May 08, 2023
Expiry Date
May 08, 2028
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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 07eb66dbddfcf36ec7a952519e49a762 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, KAKOGAWA FACTORY, SYSMEX CORPORATION;; SYSMEX CORPORATION, I-SQUARE, 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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