Taiwan FDA registration 68700ffddde735424f13dd6521548f0d
"Siemens" special chemical corrector
TW: “西門子”特殊化學校正品
Taiwan·Risk Class 2·SIEMENS HEALTHCARE DIAGNOSTICS INC.;; RANDOX LABORATORIES LTD.·Registered Aug 22, 2008 – Aug 22, 2028ActiveRegistration details
- Analysis ID
- 68700ffddde735424f13dd6521548f0d
- Customs Code
- DHA00601942800
Company information
- Manufacturer Country
- United Kingdom;;United States
- Authorized Representative
- SIEMENS HEALTHCARE LIMITED
Product details
- Intended Use
- In vitro diagnostic tests for the calibration of the ADVIA biochemical analysis system for the detection of acid phosphoric acid per (total and non-prostate), lactic acid, lipolysis per and total iron-binding capacity (TIBC), and for the calibration of the ADVIA IMS system for the detection of lipolysis per of the in vitro.
- 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
- Aug 22, 2008
- Expiry Date
- Aug 22, 2028
About this record
Access comprehensive regulatory information for "Siemens" special chemical corrector in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 68700ffddde735424f13dd6521548f0d and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS INC.;; RANDOX LABORATORIES LTD.. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.
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