Taiwan FDA registration 94730bf3169099cd8aaaecd1d96877d6
Practical Erliqi Urinary Bilinogen Confirmation Reagent (Unsterilized)
TW: 實用 爾利其尿膽原確認試劑 (未滅菌)
Taiwan·Risk Class 1·SHIH-YUNG MEDICAL INSTRUMENTS CO., LTD.·Registered Aug 24, 2007 – Aug 24, 2027ActiveRegistration details
- Analysis ID
- 94730bf3169099cd8aaaecd1d96877d6
- Customs Code
- DHY04300197407
Company information
- Manufacturer
- SHIH-YUNG MEDICAL INSTRUMENTS CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- SHIH-YUNG MEDICAL INSTRUMENTS CO., LTD.
Product details
- Intended Use
- It is limited to the first level of identification scope of the urethral urobilin salt (non-quantitative) test system (A.1785) of the classification and grading management measures for medical devices.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1785 Urethral urobilin salt (non-quantitative) test system
- Import Information
- Domestic
Dates and status
- Registration Date
- Aug 24, 2007
- Expiry Date
- Aug 24, 2027
About this record
Access comprehensive regulatory information for Practical Erliqi Urinary Bilinogen Confirmation Reagent (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 94730bf3169099cd8aaaecd1d96877d6 and manufactured by SHIH-YUNG MEDICAL INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is SHIH-YUNG MEDICAL INSTRUMENTS CO., LTD..
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