Taiwan FDA registration 043e9d7072fca2f6a4f4b456c4bb89ac

"Siemens" uric acid reagent (unsterilized)

TW: "西門子" 尿酸試劑 (未滅菌)

Taiwan·Risk Class 1·RANDOX LABORATORIES LIMITED;; SIEMENS HEALTHCARE DIAGNOSTICS INC.·Registered Aug 30, 2017 – Aug 30, 2027Active

Registration details

Analysis ID: 043e9d7072fca2f6a4f4b456c4bb89ac
Customs Code: DHA09401825003

Company information

Manufacturer: RANDOX LABORATORIES LIMITED;; SIEMENS HEALTHCARE DIAGNOSTICS INC.
Manufacturer Country: United Kingdom;;United States
Authorized Representative: SIEMENS HEALTHCARE LIMITED

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: Contract manufacturing;; input

Dates and status

Registration Date: Aug 30, 2017
Expiry Date: Aug 30, 2027

About this record

Access comprehensive regulatory information for "Siemens" uric acid 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 043e9d7072fca2f6a4f4b456c4bb89ac and manufactured by RANDOX LABORATORIES LIMITED;; SIEMENS HEALTHCARE DIAGNOSTICS INC.. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.

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