No image

EPO (Erythropoietin) ELISA

EIA-3646 · DRG Instruments Gesellschaft mit beschränkter Haftung

The EPO ELISA is intended for in vitro diagnostic use in the quantitative determination of Erythropoietin (EPO) in human serum

Details

Device typeErythropoietin (EPO) IVD, reagent: A substance or reactant intended to be used together with a parent IVD to perform a specific function in an assay that is used for the quantitative measurement of erythropoietin (EPO) in a clinical specimen.

FDA categoryAssay, Erythropoietin

Device ID04048474036466

Catalog numberEIA-3646

AvailabilityPrescription

Single useYes

MRI safetyLabeling does not contain MRI Safety Information

Contact

Phone973-564-7555

Emailcorp@drg-international.com

Related products

Product	Model	Company	Device type
Dehydroepiandrosterone (DHEA) ELISAAmerican Laboratory Products Company, Ltd.Dehydroepiandrosterone (DHEA) IVD, kit, enzyme immunoassay (EIA)	11-HEAHU-E01	American Laboratory Products Company, Ltd.	Dehydroepiandrosterone (DHEA) IVD, kit, enzyme immunoassay (EIA)
Pregnenolone ELISAEUROIMMUN Medizinische Labordiagnostika AGPregnenolone IVD, kit, enzyme immunoassay (EIA)	EQ 6164-9601	EUROIMMUN Medizinische Labordiagnostika AG	Pregnenolone IVD, kit, enzyme immunoassay (EIA)
Pregnenolone Direct ELISADRG International IncPregnenolone IVD, kit, chemiluminescent immunoassay	EIA-4170	DRG International Inc	Pregnenolone IVD, kit, chemiluminescent immunoassay
Progesterone, 17 a-Hydroxy- (Neonate) (MW) ELISADRG International Inc17-Hydroxyprogesterone IVD, kit, chemiluminescent immunoassay	EIA-1429	DRG International Inc	17-Hydroxyprogesterone IVD, kit, chemiluminescent immunoassay