Pure Global

Beckman Coulter fructosamine assay reagent - Taiwan Registration e44ae16a904ea614d92fcb42e585b47e

Access comprehensive regulatory information for Beckman Coulter fructosamine 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 e44ae16a904ea614d92fcb42e585b47e and manufactured by SENTINEL CH. SPA. The authorized representative in Taiwan is BECKMAN COULTER TAIWAN INC., TAIWAN BRANCH (U.S.A.).

This page provides complete technical specifications, regulatory compliance details. 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
e44ae16a904ea614d92fcb42e585b47e
Registration Details
Taiwan FDA Registration: e44ae16a904ea614d92fcb42e585b47e
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

Beckman Coulter fructosamine assay reagent
TW: ่ฒๅ…‹ๆ›ผๅบซ็ˆพ็‰นๆžœ็ณ–่ƒบๆชข้ฉ—่ฉฆๅŠ‘
Risk Class 2

Registration Details

e44ae16a904ea614d92fcb42e585b47e

DHA05603488607

Company Information

Product Details

This product uses kinetic colorimetry to detect fructosamine concentration in human serum or plasma.

B Haematology, pathology and genetics; A Clinical chemistry and clinical toxicology

A.1660 Quality control materials (analytical and non-analytical); A.1150 calibration;; B.7470 Analysis of glycosylated hemoglobin

Input;; QMS/QSD

Dates and Status

Aug 06, 2021

Aug 06, 2026