"Siemens" antithyroglobulin reagent group
Taiwan·Risk Class 2·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Registered Jun 17, 2022 – Jun 17, 2027Active- Analysis ID
- fd43f62518ae84878630733a9b8a3ba2
- Customs Code
- DHA05603566407
- Manufacturer
- SIEMENS HEALTHCARE DIAGNOSTICS INC.
- Manufacturer Country
- United States
- Authorized Representative
- SIEMENS HEALTHCARE LIMITED
- Intended Use
- This product is used for in vitro diagnostics, and needs to be used with ADVIA Centaur XP Systems, ADVIA Centaur XPT Systems, and ADVIA Centaur CP Systems to quantitatively detect thyroglobulin autoantibody content in serum or plasma.
- Product Type (Level 1)
- A Clinical Chemistry and Clinical Toxicology;; C Immunology and Microbiology
- Product Type (Level 2)
- C.5870 Cypress of the Upper Gland; A.1660 Grade Material (Analysis Material Non-Analysis);; A.1150 Calibrated Products
- Import Information
- Input;; QMS/QSD
- Registration Date
- Jun 17, 2022
- Expiry Date
- Jun 17, 2027
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Access comprehensive regulatory information for "Siemens" antithyroglobulin reagent group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fd43f62518ae84878630733a9b8a3ba2 and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS INC.. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.
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