Diamond Logo
Diamond Logo
Consumables - Beckman LX, DXC Series

LX, LX Pro, DXC, DXC Pro series

Diamond Diagnostics is the pioneer and clear global leader in the manufacture and supply of high quality, cost-effective alternative consumables for Beckman.

High Quality Alternative
Direct, Drop-in Replacement Products
2-3 Years Expiration on all Reagents
FDA 510k Cleared, ISO Certified, CE Marked
Bulk and OEM Options Available


 FDA 510k Cleared, ISO Certified, CE Marked

Reagents & Controls
Diamond No.Product DescriptionModelsUOMPrice
BK-467915DISE BufferAll Models2X2L
BK-467935DISE ReferenceAll Models2X2L
BK-472481DCO2 Acid ReagentAll Models2X2L
BK-472515DCO2 Alkaline ReagentAll Models500ML
BK-472482DBUN ReagentAll Models2X2L
BK-472500DGlucose ReagentAll Models2X2L
BK-472525DCreatinine ReagentAll Models2X2L
BK-467868DPhosphorous ReagentAll Models2X2L
BK-467858DAlbumin ReagentAll Models2X2L
BK-465986DTotal Protein ReagentAll Models2X2L
BK-445865DWash Concentrate IIDXC 600-8002X2L

Electrodes & Accessories
Diamond No.Product DescriptionModelsUOMPrice
BK-668295DNa+ ElectrodeAll ModelsEA
BK-669114DK+ ElectrodeAll ModelsEA
BK-669115DK+ Body ElectrodeAll ModelsEA
BK-669117DK+ Tip ElectrodeAll ModelsEA
BK-467769DCa++ ElectrodeAll ModelsEA
BK-441930DCl- ElectrodeAll ModelsEA
BK-660318DCO2 ElectrodeAll ModelsEA
BK-661750DCO2 MembraneAll ModelsPK-5
BK-651940DBUN ElectrodeAll ModelsEA
BK-469499DGlucose ElectrodeAll ModelsEA
BK-670597DGlucose Electrode MembraneAll ModelsPK-25

∞ For further information contact Customer Service - CS@diamonddiagnostics.com or call (508) 429-0450.
∞ Pricing subject to change without notice. Minimum order is $50.

Contact Us

Corporate Headquarters (USA)
Diamond Diagnostics Inc.
333 Fiske Street
Holliston, MA 01746-2048
Tel: +1 508.429.0450

Distribution Center (EU)
Diamond Diagnostics Kft.
1044 Budapest, Hungary
Óradna Street 6
Tel: +36 (1) 787 2222


ISO 9001:2015 (US)
ISO 9001:2015 (EU)
ISO 13485:2016 (US)
ISO 13485:2016 (EU)

Diamond Diagnostics Inc. is registered with the United States Food and Drug Administration as an Initial Importer Manufacturer and Contract Manufacturer. Establishment registration and device listing can be found under ID: 3003030793.

Diamond has been registered with the Food and Drug Administration since 2001 and regulated by its cGMP system requirements.

All products manufactured by Diamond carry the necessary FDA clearance and comply to the European Union IVD Directive. Every department and function in our company is standardized, controlled and routinely audited.

FDA logo

The names and logos of manufacturers, their instruments, and their products referred to herein may be protected by trademark or other law, and are used herein solely for purpose of reference. Products are available for international distribution only unless otherwise indicated. Diamond Diagnostics expressly disclaims any affiliation with products it does not manufacture, as well as sponsorship by other manufacturers. For current regulatory status on products within this website, please contact your sales representative. Prices and Information shown are for reference only and may change without notice. SmartLyte®, ProLyte®, CareLyte®, and Down-To-Frame® Refurbishing are Registered Trademarks of Diamond Diagnostics®.

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