Taiwan FDA registration 5ae44a39419932911974becdc15fc697
Wei Di Automatic Urinalysis System (Unsterilized)
TW: 偉廸 自動尿液分析系統 (未滅菌)
Taiwan·Risk Class 1·YD DIAGNOSTICS CORPORATION·Registered Dec 21, 2021 – Oct 31, 2025ExpiredRegistration details
- Analysis ID
- 5ae44a39419932911974becdc15fc697
- Customs Code
- DHA084a0002806
Company information
- Manufacturer
- YD DIAGNOSTICS CORPORATION
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- TUNYEN ENTERPRISE CORPORATION
Product details
- Intended Use
- 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.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.2900 Automated urinalysis system
Dates and status
- Registration Date
- Dec 21, 2021
- Expiry Date
- Oct 31, 2025
About this record
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.
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