Taiwan FDA registration 297c33d57973ddac3d63d90eaa7a8e41

"Siemens" thyroglobulin autologous antibody reagent

TW: "西門子" 甲狀腺球蛋白自體抗體試劑組
Taiwan flagTaiwan·Risk Class 2·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Registered Dec 01, 2005 – Dec 01, 2025Expired
Registration details
Analysis ID
297c33d57973ddac3d63d90eaa7a8e41
Customs Code
DHA00601515800
Company information
Manufacturer Country
United States
Authorized Representative
SIEMENS HEALTHCARE LIMITED
Product details
Intended Use
This product is suitable for ADVIA Centaur, ADVIA Centaur XP, ADVIA Centaur CP analyzer to quantitatively determine the concentration of thyroglobulin autoantibodies in serum or EDTA-containing plasma.
Product Type (Level 1)
C Immunology and microbiology
Import Information
import
Dates and status
Registration Date
Dec 01, 2005
Expiry Date
Dec 01, 2025
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About this record

Access comprehensive regulatory information for "Siemens" thyroglobulin autologous antibody reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 297c33d57973ddac3d63d90eaa7a8e41 and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS INC.. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.

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