The Diamond Diagnostics SmartLyte® Plus Electrolyte Analyzer is a completely automated system measuring Na+, K+, Cl-, Ca++ and Li+ in whole blood, serum, plasma and urine utilizing Ion Selective Electrode (ISE) technology. The Diamond SmartLyte® Plus is uniquely designed with a powerful microprocessor allowing for easy interface with external LIS systems, operation with a new touch screen interface, bar code scanner and storage and retrieval of over 10,000 patient results. The system currently operates in over 12 languages and offers laboratories the option to utilize the analyzer for either human or veterinary applications.
|User Input||Data Storage||Connectivity|
|5” Touch Screen||10,000 Patient Results||LAN, Wifi, 4 USB ports|
|Remote Access||10,000 QC Results per Level||RS232, LIS|
|Analysis Time||Support||Number of Parameters|
|28 sec (512/hour)||Online Service Interface||5 Total 4 (Simultaneously)|
|Calibration||Sample Size||Veterinary Options|
|2 Point every 4 hours||Whole Blood, Serum (95 µl)||Feline, Canine, Bovine,|
|1 Point every sample||Plasma, QCs (95 µl)||Equine, Swine, Ovine,|
|On Demand||Urine (180 µl)||Murine or Open|
|English, 中文, Español,||日本語, 한국어, Português,|
|Français, Deutsch,||Polskie, Русский, Türkçe|
|Indonesia, Italian, 日本語,|
User Friendly Navigation
|Extensive Onscreen Diagnostics||Simple Search Function||Easily Access Data and Results|
Parameters and Specifications
|Serum Na+||40-200 mmol/L||CV ≤ 1% (120-160 mol/L)||0.1 mmol/L|
|Serum K+||1.7-15 mmol/L||CV ≤ 1.5% (2.5-6 mmol/L)||0.01 mmol/L|
|Serum CL-||50-200 mmol/L||CV ≤ 1% (85-130 mmol/L)||0.1 mmol/L|
|Serum Ca++||0.3-5.0 mmol/L||SD ≤ 0.02 mmol/L (0.8-1.5 mmol/L)||0.001 mmol/L|
|Serum Li+||0.2-5.5 mmol/L||SD ≤ 0.03 mmol/L (0.4-1.3 mmol/L)||0.001 mmol/L|
|Urine** Na+||3-300 mmol/L||CV ≤ 5% (100-250 mmol/L)||0.1 mmol/L|
|Urine** K+||5-120 mmol/L***||CV ≤ 5% (10-60 mmol/L)||0.01 mmol/L|
|Urine** CL-||15-300 mmol/L||CV ≤ 5% (100-250 mmol/L)||0.1 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||13.2 x 12.4 x 12 in||Room temperature:|
|(self adjusting)||or 335 x 315 x 295 mm||15-32°C/60-90°F|
|11.6 A max, 50 Watts max||14 lbs or 6 kgs||Humidity <85%|
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
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®.