Taiwan FDA registration ee5b63b8ffe032b26357ca355ed6cc19
"Siemens" immunoglobulin M_2 reagent
TW: “西門子”免疫球蛋白M_2試劑組
Taiwan·Risk Class 2·RANDOX LABORATORIES LIMITED;; SIEMENS HEALTHCARE DIAGNOSTICS INC.·Registered Jan 23, 2008 – Jan 23, 2028ActiveRegistration details
- Analysis ID
- ee5b63b8ffe032b26357ca355ed6cc19
- Customs Code
- DHA00601893700
Company information
- Manufacturer Country
- United Kingdom;;United States
- Authorized Representative
- SIEMENS HEALTHCARE LIMITED
Product details
- Intended Use
- Quantitative determination of immunoglobulin M (IgM) 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 23, 2008
- Expiry Date
- Jan 23, 2028
About this record
Access comprehensive regulatory information for "Siemens" immunoglobulin M_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 ee5b63b8ffe032b26357ca355ed6cc19 and manufactured by RANDOX LABORATORIES LIMITED;; SIEMENS HEALTHCARE DIAGNOSTICS INC.. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.
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