The Diamond Diagnostics ProLyte® Electrolyte Analyzer is a completely automated system measuring Na+, K+, Li+ and Cl- in whole blood, serum, plasma and urine utilizing Ion Selective Electrode (ISE) technology. The Diamond ProLyte® was uniquely designed with the user in mind. With the 4” touch screen display or USB keyboard, easily navigate menus, search patient results, run on-screen diagnostics and access data remotely.
Economical, Accurate and Easy to Maintain. Perfect for any size Lab.
|45 sec (240/hour)||Online Service Interface||LAN, Wifi, 4 USB ports, RS232, LIS|
|User Input||Calibration||Sample Size|
|4” Touch Screen||2 Point every 4 hours||Whole Blood, Serum (100 µl)|
|External Keyboard||1 Point every sample||Plasma, QCs (100 µl)|
|Remote Access||On Demand||Urine (350 µl)|
|Number of Parameters||Data Storage|
|Na+ K+ Cl- L+||10,000+ Patient Results|
|4 Total / 3 (Simultaneously)||20,000+ QC Results per Level|
|English, 中文, Español,||日本語, 한국어, Português,|
|Français, Deutsch,||Polskie, Русский, Türkçe|
|Indonesia, Italian, 日本語,|
User Friendly Navigation
|Easy Access to Data/Results||One Touch Calibration||Simple Search Function||Onscreen System Diagnostics|
Parameters and Specifications
|Serum Na+||45-205 mmol/L||CV ≤ 1% (120-160 mol/L)||0.01 mmol/L|
|Serum K+||1.5-15 mmol/L||CV ≤ 1.5% (2.5-6 mmol/L)||0.01 mmol/L|
|Serum CL-||45-205 mmol/L||CV ≤ 1% (85-130 mmol/L)||0.01 mmol/L|
|Serum Li+||0.15-5.00 mmol/L||SD ≤ 0.03 mmol/L (0.4-1.3 mmol/L)||0.001 mmol/L|
|Urine** Na+||30-1020 mmol/L||CV ≤ 5% (100-250 mmol/L)||0.01 mmol/L|
|Urine** K+||20-505 mmol/L***||CV ≤ 5% (10-60 mmol/L)||0.01 mmol/L|
|Urine** CL-||25-505 mmol/L||CV ≤ 5% (100-250 mmol/L)||0.01 mmol/L|
|*Typical Within Run (n=30) Blood, Serum, Plasma|
|**Calcium and Lithium are not typically measured in urine samples|
|***(60-120) requires additional dilution|
|Power||Size & Weight||Ambient Conditions|
|100-240V ~ 50/60 Hz||9.5” (24cm) W x 16.5” (42cm)||Room temperature:|
|(self adjusting)||14 lbs or 6 kgs||15-32°C/60-90°F|
|1.6 A max, 50 Watts max||Humidity <85%|
Corporate Headquarters (USA)
Diamond Diagnostics Inc.
333 Fiske Street
Holliston, MA 01746-2048
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.
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®.