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Taiwan FDA registration 5860d90877089e9d7a793c8c676c4bdb

Beckman Coulter Automated Urinalysis System (Non-Sterile)

TW: 貝克曼庫爾特 自動尿液分析系統 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·BECKMAN COULTER, INC.·Registered Aug 12, 2024 – Oct 31, 2025Expired
Registration details
Analysis ID
5860d90877089e9d7a793c8c676c4bdb
Customs Code
DHA084A0029605
Company information
Manufacturer
BECKMAN COULTER, INC.
Manufacturer Country
United States
Authorized Representative
BECKMAN COULTER TAIWAN INC., TAIWAN BRANCH (U.S.A.)
Product details
Intended Use
It is limited to the first level of identification of the "Automated Urinalysis System (A.2900)" for the classification and grading management of medical devices.
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A.2900 Automated urinalysis system
Import Information
import
Dates and status
Registration Date
Aug 12, 2024
Expiry Date
Oct 31, 2025
About this record

Access comprehensive regulatory information for Beckman Coulter Automated Urinalysis System (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5860d90877089e9d7a793c8c676c4bdb and manufactured by BECKMAN COULTER, INC.. The authorized representative in Taiwan is BECKMAN COULTER TAIWAN INC., TAIWAN BRANCH (U.S.A.).

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