Taiwan FDA registration 9f0170bf4af95e2ae25e3b5d1d7733b2
Imin prolactin radioimmunoassay reagent
TW: 伊敏催乳激素放射免疫分析試劑
Taiwan·Risk Class 2·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Registered Nov 16, 2005 – Nov 16, 2015CancelledRegistration details
- Analysis ID
- 9f0170bf4af95e2ae25e3b5d1d7733b2
- Customs Code
- DHAS0601476001
Company information
- Manufacturer
- SIEMENS HEALTHCARE DIAGNOSTICS INC.
- Manufacturer Country
- United States
- Authorized Representative
- ALICE LEE INDUSTRIES CO., LTD.
Product details
- Intended Use
- Immunoradiological analysis labeled 125I was used to quantify the concentration of prolactin in human serum.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- 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
- Nov 16, 2005
- Expiry Date
- Nov 16, 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 prolactin 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 9f0170bf4af95e2ae25e3b5d1d7733b2 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