Taiwan FDA registration 54b4ad0cced070c6c3e7148eaf5167ce
Imin triiodothyroxine radioimmunoassay reagent
TW: 伊敏三碘甲狀腺素放射免疫分析試劑
Registration details
- Analysis ID
- 54b4ad0cced070c6c3e7148eaf5167ce
- Customs Code
- DHAS0601505501
Company information
- Manufacturer
- SIEMENS HEALTHCARE DIAGNOSTICS INC.
- Manufacturer Country
- United States
- Authorized Representative
- ALICE LEE INDUSTRIES CO., LTD.
Product details
- Intended Use
- Solid-state 125I radioimmunoassay is used to detect the status of the thyroid gland in human serum or plasma.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1715 Triiodothyroxine absorption test system
- 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 27, 2005
- Expiry Date
- Nov 27, 2015
- 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 Imin triiodothyroxine 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 54b4ad0cced070c6c3e7148eaf5167ce and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS INC.. The authorized representative in Taiwan is ALICE LEE INDUSTRIES CO., LTD..
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