Taiwan FDA registration 5eed3b9441133d5d2635b03a656e1c4d
Wei Di urine test strip
TW: 偉廸尿液檢驗試紙
Registration details
- Analysis ID
- 5eed3b9441133d5d2635b03a656e1c4d
- Customs Code
- DHA00601896301
Company information
- Manufacturer
- YD DIAGNOSTICS CORPORATION
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- TUNYEN ENTERPRISE CORPORATION
Product details
- Intended Use
- Determination of one to more of the following parameters in urine: red blood cells, bilirubin, urobilinogen, ketone bodies, protein, nitrite acid, glucose, pH, specific gravity, white blood cells and ascorbic acid.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1095 Ascorbic acid test system
- Import Information
- import
Dates and status
- Registration Date
- Mar 05, 2008
- Expiry Date
- Mar 05, 2028
About this record
Access comprehensive regulatory information for Wei Di urine test strip in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5eed3b9441133d5d2635b03a656e1c4d and manufactured by YD DIAGNOSTICS CORPORATION. The authorized representative in Taiwan is TUNYEN ENTERPRISE CORPORATION.
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