"Sysmecon" automatic blood coagulation analyzer
- Analysis ID
- bc184aced35979837bb6ac0aa31ae08b
- Customs Code
- DHA05602831402
- Manufacturer Country
- Japan
- Authorized Representative
- SYSMEX TAIWAN CO., LTD.
- 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
- Registration Date
- Mar 24, 2016
- Expiry Date
- Mar 24, 2026
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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.