Taiwan FDA registration 6aea92df11c9ea242d89893f6d9dc5c7
"Siemens" acid phosphate per reagent group
TW: “西門子”酸性磷酸每試劑組
Taiwan·Risk Class 2·RANDOX LABORATORIES LIMITED;; SIEMENS HEALTHCARE DIAGNOSTICS INC.·Registered Jan 22, 2008 – Jan 22, 2018CancelledRegistration details
- Analysis ID
- 6aea92df11c9ea242d89893f6d9dc5c7
- Customs Code
- DHA00601893305
Company information
- Manufacturer Country
- United Kingdom;;United States
- Authorized Representative
- SIEMENS HEALTHCARE LIMITED
Product details
- Intended Use
- For in vitro diagnostics. The total prostate acid phosphate per and non-prostate acid phosphate per non-prostate source in human serum was quantified on the ADVIA automated chemical analysis system.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1020 Acid phosphatase (total or prostate) testing system
- Import Information
- import
Dates and status
- Registration Date
- Jan 22, 2008
- Expiry Date
- Jan 22, 2018
- Cancellation Date
- Nov 04, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Siemens" acid phosphate per 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 6aea92df11c9ea242d89893f6d9dc5c7 and manufactured by RANDOX LABORATORIES LIMITED;; SIEMENS HEALTHCARE DIAGNOSTICS INC.. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.
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