Taiwan FDA registration 853c30dfeabf3d3b34f748d148c8c08d
"Siemens" androstenedione radioimmunoassay reagent
TW: “西門子”雄烯二酮放射免疫分析試劑
Taiwan·Risk Class 2·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Registered Jan 18, 2013 – Jan 18, 2018CancelledRegistration details
- Analysis ID
- 853c30dfeabf3d3b34f748d148c8c08d
- Customs Code
- DHAS0602431805
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 androstenedione levels in human serum, EDTA blood and heparinized blood cells.
- 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
- Jan 18, 2013
- Expiry Date
- Jan 18, 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" androstenedione 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 853c30dfeabf3d3b34f748d148c8c08d and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS INC.. The authorized representative in Taiwan is SIEMENS LIMITED.
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices