Taiwan FDA registration c38acde73d67c9b7dbcdb0e971f15883
Bio-researched uric acid reagent (N) (unsterilized)
TW: 生研尿酸試劑(N) (未滅菌)
Taiwan·Risk Class 1·DENKA SEIKEN CO., LTD. KAGAMIDA FACTORY·Registered Aug 30, 2006 – Aug 30, 2016CancelledRegistration details
- Analysis ID
- c38acde73d67c9b7dbcdb0e971f15883
- Customs Code
- DHA04400510009
Company information
- Manufacturer
- DENKA SEIKEN CO., LTD. KAGAMIDA FACTORY
- Manufacturer Country
- Japan
- Authorized Representative
- TUNYEN ENTERPRISE CORPORATION
Product details
- Intended Use
- Limited to the first level identification range of the "uric acid test system (A.1775)" of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1775 尿酸試驗系統
- Import Information
- import
Dates and status
- Registration Date
- Aug 30, 2006
- Expiry Date
- Aug 30, 2016
- Cancellation Date
- Aug 29, 2016
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for Bio-researched uric acid reagent (N) (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c38acde73d67c9b7dbcdb0e971f15883 and manufactured by DENKA SEIKEN CO., LTD. KAGAMIDA FACTORY. The authorized representative in Taiwan is TUNYEN ENTERPRISE CORPORATION.
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