Taiwan FDA registration 01dff3737bd86c89f7f449d5fd7373e5
Iminandrostenedione radioimmunoassay reagent
TW: 伊敏雄烯二酮放射免疫分析試劑
Taiwan·Risk Class 1·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Registered Nov 14, 2011 – Nov 14, 2016CancelledRegistration details
- Analysis ID
- 01dff3737bd86c89f7f449d5fd7373e5
- Customs Code
- DHAS0602274208
Company information
- Manufacturer
- SIEMENS HEALTHCARE DIAGNOSTICS INC.
- Manufacturer Country
- United States
- Authorized Representative
- ALICE LEE INDUSTRIES CO., LTD.
Product details
- Intended Use
- Radioimmunoassay was used to quantify the androstenedione levels in human serum and blood.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1075 雄固烯二酮試驗系統
- Import Information
- Input;; Consent letter must be attached to the import (consent from the Atomic Energy Commission must be obtained for each import)
Dates and status
- Registration Date
- Nov 14, 2011
- Expiry Date
- Nov 14, 2016
- Cancellation Date
- Jul 31, 2018
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for Iminandrostenedione radioimmunoassay reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 01dff3737bd86c89f7f449d5fd7373e5 and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS INC.. The authorized representative in Taiwan is ALICE LEE INDUSTRIES CO., LTD..
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