Taiwan FDA registration 1171089f901a85c91212140e2e4a86c2
"Wei Di" urine ketone test strip (unsterilized)
TW: "偉廸" 尿液酮體檢驗試紙 (未滅菌)
Registration details
- Analysis ID
- 1171089f901a85c91212140e2e4a86c2
- Customs Code
- DHA04401177906
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 "Ketone (Non-quantitative) Test System (A.1435)" of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1435 Ketone (non-quantitative) testing system
- Import Information
- import
Dates and status
- Registration Date
- Jun 01, 2012
- Expiry Date
- Jun 01, 2017
- Cancellation Date
- Jun 27, 2017
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Wei Di" urine ketone 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 1171089f901a85c91212140e2e4a86c2 and manufactured by YD DIAGNOSTICS CORPORATION. The authorized representative in Taiwan is TUNYEN TECHNOLOGY 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