Taiwan FDA registration 588c641b6dbe4c540de265dbd5687db9
Wei Di Automatic Urine Analyzer (Unsterilized)
TW: 偉廸自動尿液分析儀(未滅菌)
Taiwan·Risk Class 1·YD DIAGNOSTICS CORPORATION·Registered Apr 03, 2008 – Apr 03, 2023CancelledRegistration details
- Analysis ID
- 588c641b6dbe4c540de265dbd5687db9
- Customs Code
- DHA04400662702
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)
- A.2900 Automated urinalysis system
- Import Information
- import
Dates and status
- Registration Date
- Apr 03, 2008
- Expiry Date
- Apr 03, 2023
- Cancellation Date
- Sep 30, 2021
Cancellation information
- Status
- Logged out
- Reason
- 轉為登錄字號
About this record
Access comprehensive regulatory information for Wei Di Automatic Urine Analyzer (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 588c641b6dbe4c540de265dbd5687db9 and manufactured by YD DIAGNOSTICS CORPORATION. The authorized representative in Taiwan is TUNYEN TECHNOLOGY CORPORATION.
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