Taiwan FDA registration ce72255d5a5066e858a83f51ed457e17

Beckman Coulter homocysteine assay reagent

TW: 貝克曼庫爾特同半胱胺酸分析試劑
Taiwan flagTaiwan·Risk Class 2·Axis-Shield Diagnostics Limited·Registered Apr 07, 2017 – Apr 07, 2027Active
Registration details
Analysis ID
ce72255d5a5066e858a83f51ed457e17
Customs Code
DHA05602953803
Company information
Manufacturer Country
United Kingdom
Product details
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
Dates and status
Registration Date
Apr 07, 2017
Expiry Date
Apr 07, 2027
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About this record

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.

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