Taiwan FDA registration 768ba6739f1df8c8e57de919e67dffcb
"Siemens" dehydroisandrosterone hormone radioimmunoassay reagent
TW: “西門子”脫氫異雄固酮激素放射免疫分析試劑
Taiwan·Risk Class 2·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Registered Jan 21, 2013 – Jan 21, 2018CancelledRegistration details
- Analysis ID
- 768ba6739f1df8c8e57de919e67dffcb
- Customs Code
- DHAS0602432107
Company information
- Manufacturer
- SIEMENS HEALTHCARE DIAGNOSTICS INC.
- Manufacturer Country
- United States
- Authorized Representative
- SIEMENS LIMITED
Product details
- Intended Use
- Radioimmunoassay was used to quantitatively measure the DHEA-SO4 levels in human serum and blood.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1245 Dehydroepiandrosterone (Free and Sulfur Salt) Test System
- Import Information
- Consent must be attached to the import (with the consent of the Atomic Energy Commission must be obtained for each import); input
Dates and status
- Registration Date
- Jan 21, 2013
- Expiry Date
- Jan 21, 2018
- Cancellation Date
- Dec 13, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Siemens" dehydroisandrosterone hormone radioimmunoassay reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 768ba6739f1df8c8e57de919e67dffcb and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS INC.. The authorized representative in Taiwan is SIEMENS LIMITED.
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