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Beckman Coulter Automated Urinalysis System (Non-Sterile) - Taiwan Registration 5860d90877089e9d7a793c8c676c4bdb

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.).

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.

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5860d90877089e9d7a793c8c676c4bdb
Registration Details
Taiwan FDA Registration: 5860d90877089e9d7a793c8c676c4bdb
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Device Details

Beckman Coulter Automated Urinalysis System (Non-Sterile)
TW: ่ฒๅ…‹ๆ›ผๅบซ็ˆพ็‰น ่‡ชๅ‹•ๅฐฟๆถฒๅˆ†ๆž็ณป็ตฑ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

5860d90877089e9d7a793c8c676c4bdb

DHA084A0029605

Company Information

United States

Product Details

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.

A Clinical chemistry and clinical toxicology

A.2900 Automated urinalysis system

import

Dates and Status

Aug 12, 2024

Oct 31, 2025