Routine Clinical Chemistry
Support everyday laboratory testing requirements with clinical chemistry solutions designed for routine diagnostic workflows.
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Quality Control Materials
AV-QCURINE AV-QC Urine Chemistry Control (Multi-Level Liquid)
Multi-level liquid quality control for quantitative urine chemistry assays (creatinine, urea, uric acid, protein, glucose, electrolytes and related parameters). Human-based matrix with extended open-vial stability. Designed by Aurevant Medical for reliable monitoring of urine chemistry methods on automated and semi-automated analyzers.
No approved datasheet is available for this product yet.
Product Overview
Overview
The Aurevant AV-QC Urine Chemistry Control is a liquid, ready-to-use multi-level quality control material formulated for the monitoring of precision and accuracy of quantitative urine chemistry assays. It is intended for use with methods that measure urine creatinine, urea, uric acid, total protein, glucose, selected electrolytes and other commonly requested urine chemistry parameters.
The control is prepared in a human-based urine matrix to provide good commutability with patient urine samples. Being liquid and ready-to-use, it requires no reconstitution, reducing preparation time and the risk of reconstitution errors. After opening, the material demonstrates extended open-vial stability when stored at the recommended temperature, supporting consistent daily or batch-wise quality-control practices.
Assayed target values and acceptable ranges are provided on a lot-specific value sheet for each level. The control is suitable for use on Aurevant AV-Chem series analyzers running urine chemistry applications as well as other open-system clinical chemistry instruments after laboratory validation.
This product is an original Aurevant Medical quality control material manufactured under controlled conditions and intended for professional laboratory use by trained personnel.
The control is prepared in a human-based urine matrix to provide good commutability with patient urine samples. Being liquid and ready-to-use, it requires no reconstitution, reducing preparation time and the risk of reconstitution errors. After opening, the material demonstrates extended open-vial stability when stored at the recommended temperature, supporting consistent daily or batch-wise quality-control practices.
Assayed target values and acceptable ranges are provided on a lot-specific value sheet for each level. The control is suitable for use on Aurevant AV-Chem series analyzers running urine chemistry applications as well as other open-system clinical chemistry instruments after laboratory validation.
This product is an original Aurevant Medical quality control material manufactured under controlled conditions and intended for professional laboratory use by trained personnel.
Product name and code identify the record only; they are not a substitute for current manufacturer documentation. Confirm intended use, configuration, availability, supported applications, and all technical and commercial terms in writing before procurement.
Key Features
Features
- •Multi-level liquid control specifically designed for urine chemistry assays
- •Human-based urine matrix for improved commutability with patient urine samples
- •Ready-to-use liquid format – no reconstitution required
- •Assayed for key urine chemistry analytes (creatinine, urea, uric acid, protein, glucose, electrolytes, etc.)
- •Extended open-vial stability at 2–8 °C
- •Lot-specific target values and acceptable ranges supplied
- •Supports daily precision monitoring and Levey-Jennings charting of urine methods
- •Compatible with Aurevant AV-Chem analyzers and other open-system urine chemistry applications after validation
- •Covers normal and pathological concentration ranges in urine
Key advantages
- •Specialized urine matrix improves commutability with real patient urine specimens compared with serum-based controls
- •Liquid format eliminates reconstitution errors and preparation time
- •Multi-level design allows monitoring across normal and pathological urine concentration ranges
- •Extended open-vial stability supports efficient daily QC without frequent replacement
- •Assayed values enable immediate use for monitoring and troubleshooting of urine chemistry methods
- •Complements serum chemistry QC materials for laboratories performing both serum and urine testing
Sample Types
- →Not applicable (quality control material)
Safety
Safety Information
For in-vitro diagnostic use only. This product contains human-source material. Although donor units were tested and found non-reactive for common infectious disease markers, handle as potentially infectious. Wear appropriate personal protective equipment (gloves, lab coat, eye protection). Store at 2–8 °C; do not freeze. Do not use after the expiry date. After opening, observe the stated open-vial stability period and discard if contamination, turbidity or precipitation is observed. Dispose of according to local laboratory and environmental regulations. Consult the package insert and Safety Data Sheet (SDS) before use.
Instructions
Directions for Use
Remove the control bottles from refrigerated storage (2–8 °C) and allow them to equilibrate to the temperature required by the analyzer if specified.
Technical Data
Specifications
Specifications
Research Status
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Publication Approval
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Technical Specification Status
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Publication Status
approved_for_publication
Specifications Status
verified
Note
Optional verification metadata; product publication does not require any fields beyond product name and model.
Use Cases
Applications
- →Daily quality control of quantitative urine chemistry assays
- →Monitoring of urine creatinine, urea, uric acid, protein, glucose and electrolyte methods
- →Precision and accuracy verification for urine chemistry testing
- →Levey-Jennings charting and application of laboratory QC rules
- →Use on fully automated and semi-automated clinical chemistry analyzers running urine applications
Renal Function Testing
Clinical chemistry applications supporting the laboratory assessment of kidney function.
View applicationApproved documentation
Downloads
No approved documents are currently associated with this product.
Product questions
Frequently Asked Questions
Which urine analytes does this control cover?
The control is assayed for urine creatinine, urea, uric acid, total protein, glucose, selected electrolytes and related urine chemistry parameters as listed on the lot-specific value sheet.
Is it ready to use?
Yes. It is a liquid, ready-to-use control. No reconstitution is required.
How many levels are available?
The product is supplied as a multi-level control (typically two or three levels covering normal and pathological ranges). Exact configuration is stated on the product label.
What is the open-vial stability?
After opening, the control typically remains stable for 14–30 days when stored at 2–8 °C. The exact claim is provided on the package insert and value sheet for each lot.
Is the matrix urine-based?
Yes. The control is prepared in a human-based urine matrix to improve commutability with patient urine samples.
Can it be used on non-Aurevant analyzers?
Yes, after the laboratory has verified the suitability of the assigned values and matrix for the specific urine chemistry methods in use.
How should the control be mixed before use?
Gently invert the bottle several times to ensure homogeneity. Avoid vigorous shaking that may introduce bubbles.
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