Taiwan FDA registration 71c308a7fd60c1dc4a74318e2f08b629
YD Urine Analyzer (Non-Sterile)
TW: 偉廸自動尿液分析儀(未滅菌)
Taiwan·Risk Class 1·MD·YD DIAGNOSTICS CORPORATION·Registered Oct 01, 2021 – Oct 31, 2023ExpiredRegistration details
- Analysis ID
- 71c308a7fd60c1dc4a74318e2f08b629
- License Form
- Ministry of Health Medical Device Import Registration No. 006627
- Customs Code
- DHA08400662702
Company information
- Manufacturer
- YD DIAGNOSTICS CORPORATION
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- TUNYEN TECHNOLOGY CORPORATION
Product details
- Intended Use
- Limited to the first level identification range of the "Automatic Urinalysis System (A.2900)" of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A2900 Automated Urinalysis System
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2023
About this record
Access comprehensive regulatory information for YD Urine Analyzer (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 71c308a7fd60c1dc4a74318e2f08b629 and manufactured by YD DIAGNOSTICS CORPORATION. The authorized representative in Taiwan is TUNYEN TECHNOLOGY CORPORATION.
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