Taiwan FDA registration c390acbd004b6f42d727059d5dc2ec82

"Abbott" TDM complex correction solution

TW: “亞培” TDM 複合校正液
Taiwan flagTaiwan·Risk Class 2·MICROGENICS CORPORATION·Registered Nov 23, 2020 – Nov 23, 2025Expired
Registration details
Analysis ID
c390acbd004b6f42d727059d5dc2ec82
Customs Code
DHA05603415902
Company information
Manufacturer Country
United States
Product details
Intended Use
Suitable for in vitro diagnostics, calibration of human serum or plasma amikacin, carbamazepine, digoxin, gentamicin, phenobarbital, phenytoin, theophylline, valproic ACID) and vancomycin analysis.
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A.1150 Calibrated Products
Import Information
QMS/QSD;; 輸入
Dates and status
Registration Date
Nov 23, 2020
Expiry Date
Nov 23, 2025
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About this record

Access comprehensive regulatory information for "Abbott" TDM complex correction solution in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c390acbd004b6f42d727059d5dc2ec82 and manufactured by MICROGENICS CORPORATION. The authorized representative in Taiwan is ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.).

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including B.R.A.H.M.S GmbH;; MICROGENICS CORPORATION, and 1 recent registrations in the same category. 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.

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