Beckman Coulter homocysteine assay reagent
- Analysis ID
- ce72255d5a5066e858a83f51ed457e17
- Customs Code
- DHA05602953803
- Manufacturer
- Axis-Shield Diagnostics Limited
- Manufacturer Country
- United Kingdom
- Authorized Representative
- BECKMAN COULTER TAIWAN INC., TAIWAN BRANCH (U.S.A.)
- Intended Use
- This product is equipped with AU400, AU480, AU680 and AU5800 analysis systems to quantitatively detect total homocysteine concentration in human serum and plasma in vitro.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1377 Urinary bladder acid, non-quantitative test system;; A.1150 Calibrated Products
- Import Information
- import
- Registration Date
- Apr 07, 2017
- Expiry Date
- Apr 07, 2027
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Access comprehensive regulatory information for Beckman Coulter homocysteine assay reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ce72255d5a5066e858a83f51ed457e17 and manufactured by Axis-Shield Diagnostics Limited. The authorized representative in Taiwan is BECKMAN COULTER TAIWAN INC., TAIWAN BRANCH (U.S.A.).
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including AXIS-SHIELD DIAGNOSTICS LTD., and 1 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.