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TECO Uritek(Non-Sterile) - Taiwan Registration 2d37ea99da451ee58d349d203d934c32

Access comprehensive regulatory information for TECO Uritek(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 2d37ea99da451ee58d349d203d934c32 and manufactured by TECO DIAGNOSTICS. The authorized representative in Taiwan is HONEST MEDICAL INC..

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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2d37ea99da451ee58d349d203d934c32
Registration Details
Taiwan FDA Registration: 2d37ea99da451ee58d349d203d934c32
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Device Details

TECO Uritek(Non-Sterile)
TW: 醫信 尿液分析儀(未滅菌)
Risk Class 1
MD

Registration Details

2d37ea99da451ee58d349d203d934c32

Ministry of Health Medical Device Import Registration No. 004341

DHA08400434100

Company Information

United States

Product Details

A Clinical chemistry and clinical toxicology

A2900 Automated Urinalysis System

Imported from abroad

Dates and Status

Oct 01, 2021

Oct 31, 2026