Taiwan FDA registration f46d6163fd0c035bc11809ec857cd5a8

"Siemens" immunoglobulin G_2 reagent

TW: “西門子”免疫球蛋白 G_2試劑組

Taiwan·Risk Class 2·RANDOX LABORATORIES LIMITED;; SIEMENS HEALTHCARE DIAGNOSTICS INC.·Registered Jan 22, 2008 – Jan 22, 2028Active

Registration details

Analysis ID: f46d6163fd0c035bc11809ec857cd5a8
Customs Code: DHA00601893509

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: For in vitro diagnostics. Quantitative determination of immunoglobulin G (IgG) in human serum and plasma on the ADVIA Automated Chemical Analysis System.
Product Type (Level 1): C Immunology and microbiology
Product Type (Level 2): C.5510 免疫球蛋白A,G,M,D及E免疫試驗系統
Import Information: import

Dates and status

Registration Date: Jan 22, 2008
Expiry Date: Jan 22, 2028

About this record

Access comprehensive regulatory information for "Siemens" immunoglobulin G_2 reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f46d6163fd0c035bc11809ec857cd5a8 and manufactured by RANDOX LABORATORIES LIMITED;; SIEMENS HEALTHCARE DIAGNOSTICS INC.. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.

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