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Siemens Clinitek Advantus Urinalysis Analyzer
Siemens Clinitek Advantus Urinalysis AnalyzerSiemens Clinitek Advantus Urinalysis Analyzer

Siemens Clinitek Advantus Urinalysis Analyzer

Item# 0-SM-CTKADVANTUS


The Siemens Clinitek Advantus Urinalysis Analyzer, provided by Siemens Healthcare Diagnostics

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Diamond Diagnostics presents the refurbished CliniTech Advantus, a Urinalysis Analyzer available in a benchtop configuration with throughput of 7 seconds/sample; up to 500 tests/hour, manufactured by Siemens. Engineered for precise and efficient analysis of urine samples, this analyzer offers advanced technology for comprehensive urinalysis testing. Equipped with a comprehensive platform, the CliniTech Advantus enables the evaluation of various urine parameters, including pH, specific gravity, protein, glucose, ketones, bilirubin, urobilinogen, nitrites, leukocytes. With its user-friendly interface and intuitive software, the CliniTech Advantus facilitates streamlined workflow and data analysis, empowering laboratory personnel to perform urinalysis assays with ease. Its reliability and accuracy make it an invaluable tool in healthcare settings, providing clinicians with critical information for diagnosing and monitoring various renal and metabolic disorders. Whether in hospital laboratories, clinics, or research facilities, the CliniTech Advantus plays a vital role in patient care by delivering timely and accurate urinalysis results. By furnishing healthcare professionals with actionable data, it enables informed decision-making and personalized treatment strategies, ultimately contributing to improved patient outcomes and overall wellness. the CliniTech Advantus stands as a trusted ally in the pursuit of better healthcare, offering consistent performance and dependable results in every analysis.

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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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