Taiwan FDA registration c44143e789988c3fb73fd6408f232339
"Wei Di" urine protein test strip (unsterilized)
TW: "偉廸" 尿液蛋白質檢驗試紙 (未滅菌)
Registration details
- Analysis ID
- c44143e789988c3fb73fd6408f232339
- Customs Code
- DHA04401068709
Company information
- Manufacturer
- YD DIAGNOSTICS CORPORATION
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- TUNYEN ENTERPRISE CORPORATION
Product details
- Intended Use
- It is limited to the first level of identification of the "Urine Protein or Albumin (Non-quantitative) Test System (A.1645)" of the Medical Device Classification and Grading Management Measures.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1645 Urine protein or albumin (non-quantitative) testing system
- Import Information
- import
Dates and status
- Registration Date
- Aug 09, 2011
- Expiry Date
- Aug 09, 2026
About this record
Access comprehensive regulatory information for "Wei Di" urine protein test strip (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c44143e789988c3fb73fd6408f232339 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 DatabasePowered by Pure Global AI89,000+ Devices