Taiwan FDA registration cf54b31a93df7a178e9780f698505f69

Desay uric acid liquid kit (unsterilized)

TW: 德賽尿酸液體試劑盒(未滅菌)

Taiwan·Risk Class 1·DIASYS DIAGNOSTIC SYSTEMS GMBH·Registered Nov 18, 2010 – Nov 18, 2025Expired

Registration details

Analysis ID: cf54b31a93df7a178e9780f698505f69
Customs Code: DHA04400952601

Company information

Manufacturer: DIASYS DIAGNOSTIC SYSTEMS GMBH
Manufacturer Country: Germany
Authorized Representative: MEDITRUST MEDICAL SERVICE & CONSULTANT CO., LTD.

Product details

Intended Use: Limited to the first level identification scope of the "uric acid test system (A.1775)" of the Measures for the Classification and Grading Management 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: Nov 18, 2010
Expiry Date: Nov 18, 2025

About this record

Access comprehensive regulatory information for Desay uric acid liquid kit (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number cf54b31a93df7a178e9780f698505f69 and manufactured by DIASYS DIAGNOSTIC SYSTEMS GMBH. The authorized representative in Taiwan is MEDITRUST MEDICAL SERVICE & CONSULTANT CO., LTD..

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