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Consumables - Beckman CX Series

CX, CX Delta, CX 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 ISO CE

 FDA 510k Cleared, ISO Certified, CE Marked

Reagents & Controls
Diamond No.Product DescriptionModelsUOMPrice
BK-A17652DElectrolyte BufferCX 3,5,7,92X2L
BK-A17657DElectrolyte Reference SolutionCX 3,5,7,92X2L
BK-A17647DCO2 Acid ReagentCX 3,5,7,92X2L
BK-443320DCO2 Alkaline BufferCX 3,5,7,9500ML
BK-443350DBUN ReagentCX 3,7,9500ML
BK-443355DGlucose ReagentCX 3,7,9500ML
BK-443340DCreatinine ReagentCX 3,7,93X2000ML
BK-443335DWash ConcentrateCX 3,5,7,96X250ML
BK-445865DWash Concentrate IICX 4,5,7,92X2L
BK-476015DProbe Rinse SolutionCX 4,5,7,96X14ML
BK-465908DCalibrator 1CX 3,5,7,96X25ML
BK-465909DCalibrator 2CX 3,5,7,96X25ML
BK-465910DCalibrator 3CX 3,5,7,96X25ML

Electrodes & Accessories
Diamond No.Product DescriptionModelsUOMPrice
BK-668295DNa+ ElectrodeCX 3,5,7,9EA
BK-669114DK+ ElectrodeCX 3,5,7,9EA
BK-669115DK+ Body ElectrodeCX 3,5,7,9EA
BK-669117DK+ Tip ElectrodeCX 3,5,7,9EA
BK-467769DCa++ ElectrodeCX 3,7,9EA
BK-441930DCl- ElectrodeCX 3,5,7,9EA
BK-660318DCO2 ElectrodeCX 3,5,7,9EA
BK-661750DCO2 MembraneCX 3,5,7,9PK-5
BK-651940DBUN ElectrodeCX 3,7,9EA
BK-469499DGlucose ElectrodeCX 3,7,9EA
BK-670597DGlucose Electrode MembraneCX 3,7,9PK-25
BK-450661DLamp Source Ca/Creatine/TPCX 3,7,9EA

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

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Diamond Diagnostics Inc.
333 Fiske Street
Holliston, MA 01746-2048
Tel: +1 508.429.0450

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

Quality

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.

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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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