Taiwan FDA registration a9ba82a2d8ef86dec8905119e363856a

"Siemens" urine total protein test reagent (unsterilized)

TW: “西門子”尿液總蛋白質試驗試劑（未滅菌）

Taiwan·Risk Class 1·SIEMENS HEALTHCARE DIAGNOSTICS INC.;; FISHER DIAGNOSTICS·Registered May 21, 2007 – May 21, 2027Active

Registration details

Analysis ID: a9ba82a2d8ef86dec8905119e363856a
Customs Code: DHA04400589101

Company information

Manufacturer: SIEMENS HEALTHCARE DIAGNOSTICS INC.;; FISHER DIAGNOSTICS
Manufacturer Country: United States
Authorized Representative: SIEMENS HEALTHCARE LIMITED

Product details

Intended Use: It is limited to the first level of identification of the "Urine Protein or Albumin (Non-quantitative) Test System (A.1645)" of the Medical Device Classification and Grading Management Measures.
Product Type (Level 1): A Clinical chemistry and clinical toxicology
Product Type (Level 2): A.1645 Urine protein or albumin (non-quantitative) testing system
Import Information: Contract manufacturing;; input

Dates and status

Registration Date: May 21, 2007
Expiry Date: May 21, 2027

About this record

Access comprehensive regulatory information for "Siemens" urine total protein test 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 a9ba82a2d8ef86dec8905119e363856a and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS INC.;; FISHER DIAGNOSTICS. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.

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