Pure Global

Wei Di Automatic Urinalysis System (Unsterilized) - Taiwan Registration 5ae44a39419932911974becdc15fc697

Access comprehensive regulatory information for Wei Di Automatic Urinalysis System (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5ae44a39419932911974becdc15fc697 and manufactured by YD DIAGNOSTICS CORPORATION. The authorized representative in Taiwan is TUNYEN ENTERPRISE CORPORATION.

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
5ae44a39419932911974becdc15fc697
Registration Details
Taiwan FDA Registration: 5ae44a39419932911974becdc15fc697
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

Wei Di Automatic Urinalysis System (Unsterilized)
TW: ๅ‰ๅปธ ่‡ชๅ‹•ๅฐฟๆถฒๅˆ†ๆž็ณป็ตฑ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

5ae44a39419932911974becdc15fc697

DHA084a0002806

Company Information

Korea, Republic of

Product Details

Limited to the first level identification range of the "Automated Urinalysis System (A.2900)" of the Measures for the Classification and Grading of Medical Devices.

A Clinical chemistry and clinical toxicology

A.2900 Automated urinalysis system

Dates and Status

Dec 21, 2021

Oct 31, 2025