Diamond Logo
Diamond Logo
Consumables - Diamond Unity

CS300B, CS400, CS600B

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

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
BM-450043DISE DiluentAll Models5X300mL
BM-409149DHitergent SolutionAll Models1L
BM-450042DISE Internal ReferenceAll Models5X600ML
BM-450041DKCl Electrolyte SolutionAll Models5X300ML
BM-620427DISE High StandardAll Models10X2ML
BM-620428DISE Low StandardAll Models10X2ML
BM-1224310DCell Clean SolutionAll Models6X2L
BM-1489828DISE CompensatorAll Models10X2ML

Electrodes & Accessories
Diamond No.Product DescriptionModelsUOMPrice
BM-371037DNa+ ElectrodeAll ModelsEA
BM-371038DK+ ElectrodeAll ModelsEA
BM-372039DCl- ElectrodeAll ModelsEA
BM-373039DReference ElectrodeAll ModelsEA
BM-70703101DSample ProbeAll ModelsEA
BM-7070926DReagent ProbeAll ModelsEA
BM-7170551DCuvettesAll ModelsPK-24
BM-409041DSample CupsAll ModelsPK-1000

∞ For further information contact Customer Service - support@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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