Taiwan FDA registration 288b7e2c8aaacc4fde1dd8a901c12815
"Siemens" urine total protein corrector
TW: “西門子”尿總蛋白校正品
Taiwan·Risk Class 2·SIEMENS HEALTHCARE DIAGNOSTICS INC.;; RANDOX LABORATORIES LTD.·Registered Jul 01, 2008 – Jul 01, 2023ExpiredRegistration details
- Analysis ID
- 288b7e2c8aaacc4fde1dd8a901c12815
- Customs Code
- DHA00601939903
Company information
- Manufacturer Country
- United Kingdom;;United States
- Authorized Representative
- SIEMENS HEALTHCARE LIMITED
Product details
- Intended Use
- In vitro diagnostic test for the detection of total urine protein by the ADVIA biochemical analysis system.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1150 Calibrated Products
- Import Information
- import
Dates and status
- Registration Date
- Jul 01, 2008
- Expiry Date
- Jul 01, 2023
About this record
Access comprehensive regulatory information for "Siemens" urine total protein corrector in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 288b7e2c8aaacc4fde1dd8a901c12815 and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS INC.;; RANDOX LABORATORIES LTD.. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.
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