Taiwan FDA registration 1d08001a3e73e62c8174ee5798bd0ea6

Abbott clinical biochemically activated aspartate transaminase assay set

TW: 亞培臨床生化活化型天門冬氨酸轉胺酶檢驗試劑組
Taiwan flagTaiwan·Risk Class 2·ABBOTT IRELAND DIAGNOSTICS DIVISION·Registered Jan 12, 2022 – Jan 12, 2027Active
Registration details
Analysis ID
1d08001a3e73e62c8174ee5798bd0ea6
Customs Code
DHA05603520402
Company information
Manufacturer Country
Ireland
Product details
Intended Use
This product is used to quantify aspartate aminotransferase in human serum or plasma on the ARCHITECT c system.
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A.1100 天門冬胺酸轉胺酶試驗系統
Import Information
QMS/QSD;; 輸入
Dates and status
Registration Date
Jan 12, 2022
Expiry Date
Jan 12, 2027
About this record

Access comprehensive regulatory information for Abbott clinical biochemically activated aspartate transaminase assay set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1d08001a3e73e62c8174ee5798bd0ea6 and manufactured by ABBOTT IRELAND DIAGNOSTICS DIVISION. The authorized representative in Taiwan is ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.).

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