Taiwan FDA registration 46903cded3f56be77aa590a38e23d4a6

Reagent for the detection of androstenedione

TW: 禮雅尚雄烯二酮檢驗試劑

Taiwan·Risk Class 2·DIASORIN INC.·Registered Jan 24, 2019 – Jan 24, 2029Active

Registration details

Analysis ID: 46903cded3f56be77aa590a38e23d4a6
Customs Code: DHA05603214102

Company information

Manufacturer: DIASORIN INC.
Manufacturer Country: United States
Authorized Representative: MEDRICH INSTRUMENT CO., LTD.

Product details

Intended Use: This product is paired with the Reich Analyzer Series for the quantitative determination of △4 androstenedione in human serum and EDTA plasma using chemical cold light immunoassay (CLIA) technology.
Product Type (Level 1): A Clinical chemistry and clinical toxicology
Product Type (Level 2): A.1660 Grade Material (Analysis Material Non-Analysis);; A.1075 雄固烯二酮試驗系統
Import Information: import

Dates and status

Registration Date: Jan 24, 2019
Expiry Date: Jan 24, 2029

About this record

Access comprehensive regulatory information for Reagent for the detection of androstenedione in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 46903cded3f56be77aa590a38e23d4a6 and manufactured by DIASORIN INC.. The authorized representative in Taiwan is MEDRICH INSTRUMENT 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.