Taiwan FDA registration f0f426f8287b576a56aeae616c00d1c5

Api aspartate transaminase assay set

TW: 亞培天門冬胺酸轉胺酶檢驗試劑組
Taiwan flagTaiwan·Risk Class 2·FISHER DIAGNOSTICS, A DIVISION OF FISHER SCIENTIFIC COMPANY, LLC, A PART OF THERMO FISHER SCIENTIFIC INC.;; ABBOTT GMBH·Registered Mar 05, 2019 – Mar 05, 2029Active
Registration details
Analysis ID
f0f426f8287b576a56aeae616c00d1c5
Customs Code
DHA05603219802
Company information
Manufacturer Country
United States;;Germany
Product details
Intended Use
This product is used with the Alinity c analyzer to quantify aspartine transaminases in human serum or plasma.
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
Contract manufacturing;; input
Dates and status
Registration Date
Mar 05, 2019
Expiry Date
Mar 05, 2029
About this record

Access comprehensive regulatory information for Api 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 f0f426f8287b576a56aeae616c00d1c5 and manufactured by FISHER DIAGNOSTICS, A DIVISION OF FISHER SCIENTIFIC COMPANY, LLC, A PART OF THERMO FISHER SCIENTIFIC INC.;; ABBOTT GMBH. 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