Taiwan FDA registration a8729e65151f195f5145a96f6e1fb216

Imin dehydroisandrosterone hormone radioimmunoassay reagent

TW: 伊敏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 Jul 26, 2011 – Jul 26, 2016Cancelled

Registration details

Analysis ID: a8729e65151f195f5145a96f6e1fb216
Customs Code: DHAS0602253006

Company information

Manufacturer: SIEMENS HEALTHCARE DIAGNOSTICS INC.
Manufacturer Country: United States
Authorized Representative: ALICE LEE INDUSTRIES CO., LTD.

Product details

Intended Use: This product uses radioimmunoassay to quantify DHEA-SO4 in human serum and plasma in vitro.
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: Jul 26, 2011
Expiry Date: Jul 26, 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 Imin 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 a8729e65151f195f5145a96f6e1fb216 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.