Home GUDID 00858724003025
ARK™ Lamotrigine Assay
Primary DI 00858724003025
Brand ARK™ Lamotrigine Assay
Company ARK DIAGNOSTICS INC
Model 5023-0001-00
Catalog number 5023-0001-00
Device description The ARK™ Lamotrigine Assay is a homogeneous enzyme immunoassay intended for the quantitative determination of Lamotrigine in human serum or plasma on automated clinical chemistry analyzers. Lamotrigine concentrations can be used as an aid in management of patients treated with Lamotrigine. The ARK™ Lamotrigine Assay consists of reagents RI anti-Lamotrigine polyclonal antibody with substrate and R2 Lamotrigine epitope labeled with bacterial G6PDH enzyme.
Published 2016-09-24
Public version status Update
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true
Single use true
Product Codes# Code, Name table Code Name ORH Lamotrigine Assay
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class ORH Lamotrigine Assay Clinical Toxicology 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 00858724003025 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, UPC-A table Source identifier GTIN-14 normalized UPC-A EAN-13 00858724003025 00858724003025 858724003025 0858724003025
GMDN Terms# Term, Definition table Term Definition Multiple anticonvulsant therapeutic drug monitoring IVD, reagent A substance or reactant intended to be used together with a parent IVD to perform a specific function in an assay intended to be used for the quantitative measurement and therapeutic monitoring of multiple anticonvulsant drugs, also known as antiepileptic drugs which may include carbamazepine, lamotrigine, phenytoin, and primidone, in a clinical specimen.
Storage And Handling# Type, Low, High table Type Low High Condition Storage Environment Temperature 2 Degrees Celsius 8 Degrees Celsius
Regulatory Flags# DUNS number 164880598 Device count 1 Kit true Lot or batch true Expiration date on label true Other Devices From This Company# Primary DI, Brand, Model table Primary DI Brand Model Catalog Published 00858724003414 ARK™ Fentanyl Calibrator 5031-0002-00 5031-0002-00 2017-04-30 00812101031599 ARK™ Ketamine II Assay 5083-0001-00 5083-0001-00 2025-12-27 00812101031605 ARK™ Ketamine II Assay 5083-0001-01 5083-0001-00 2025-12-27 00812101031612 ARK™ Ketamine II Assay 5083-0001-02 5083-0001-02 2025-12-27 00812101031629 ARK™ Ketamine II Calibrator 5083-0002-00 5083-0002-00 2025-12-27 00812101031636 ARK™ Ketamine II Calibrator (Negative) 5083-0002-01 5083-0002-01 2025-12-27 00812101031643 ARK™ Ketamine II Calibrator (50 ng/mL Cutoff) 5083-0002-02 5083-0002-02 2025-12-27 00812101031650 ARK™ Ketamine II Calibrator (100 ng/mL Cutoff) 5083-0002-03 5083-0002-03 2025-12-27 00812101031667 ARK™ Ketamine II Control (25/75) 5083-0003-00 5083-0003-00 2025-12-27 00812101031674 ARK™ Ketamine II Control (75/125) 5083-0003-01 5083-0003-01 2025-12-27 00812101031995 ARK™ Ketamine II Assay 5083-0001-03 5083-0001-03 2025-12-27 00812101031001 DRI Tramadol Assay - 500 mL B40000350 B40000350 2024-11-14 00812101031018 DRI Tramadol Assay - 115mL B40000351 B40000351 2024-11-14 00812101031025 DRI Tramadol Negative Calibrator Kit B40000353 B40000353 2024-11-14 00812101031032 DRI Tramadol Cutoff Calibrator Kit B40000352 B40000352 2024-11-14 00812101031049 DRI Tramadol Calibrator Kit B40000366 B40000366 2024-11-14 00812101031056 DRI Tramadol Control Kit B40000354 B40000354 2024-11-14 00812101031469 ARK Levetiracetam II Assay 5070-0001-01 5070-0001-01 2024-10-25 00812101030646 ARK™ Levetiracetam II Assay 5070-0001-00 5070-0001-00 2024-10-24 00812101030653 ARK™ Levetiracetam II Calibrator 5070-0002-00 5070-0002-00 2024-10-24
Other Devices Sharing Product Codes# Primary DI, Brand, Company table Primary DI Brand Company Product code Published 00884883011168 QMS Lamotrigine Immunoassay Microgenics Corporation ORH 2016-09-22 00884883012684 QMS Lamotrigine Assay Microgenics Corporation ORH 2016-09-12