Taiwan FDA registration d921c24502ffce6abf9d5c378d823a17
"DiaSys" Uric Acid FS TOOS (Non-Sterile)
TW: "德信" 尿酸試劑(未滅菌)
Taiwan·Risk Class 1·MD·DIASYS DIAGNOSTIC SYSTEMS GMBH·Registered Jul 29, 2019 – Jul 29, 2024ExpiredRegistration details
- Analysis ID
- d921c24502ffce6abf9d5c378d823a17
- License Form
- Ministry of Health Medical Device Import No. 020692
- Customs Code
- DHA09402069201
Company information
- Manufacturer
- DIASYS DIAGNOSTIC SYSTEMS GMBH
- Manufacturer Country
- Germany
- 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)
- A1775 Uric acid test system
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 29, 2019
- Expiry Date
- Jul 29, 2024
About this record
Access comprehensive regulatory information for "DiaSys" Uric Acid FS TOOS (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d921c24502ffce6abf9d5c378d823a17 and manufactured by DIASYS DIAGNOSTIC SYSTEMS GMBH. The authorized representative in Taiwan is TUNYEN ENTERPRISE CORPORATION.
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