Mindray Progesterone (CLIA)

1 INR/Unit

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Product Details:

Function Detection of progesterone levels in serum/plasma
Features High specificity and sensitivity, Ready-to-use reagents
Accuracy High, per manufacturers testing criteria
Instruments Type Compatible with Mindray CL-series analyzers
Storage Instructions Store at 2 to 8 Degree Celsius, avoid freezing
Shelf Life Up to expiration date stated on box (typically 12-18 months)
Usage Type Laboratory/Clinical
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Mindray Progesterone (CLIA) Price And Quantity

Minimum Order Quantity 1 Unit
Price 1 INR/Unit

Mindray Progesterone (CLIA) Product Specifications

Shelf Life Up to expiration date stated on box (typically 12-18 months)
Usage Type Laboratory/Clinical
Technology Chemiluminescence Immunoassay (CLIA)
Storage Instructions Store at 2 to 8 Degree Celsius, avoid freezing
Instruments Type Compatible with Mindray CL-series analyzers
Accuracy High, per manufacturers testing criteria
Real-Time Operation Yes
Features High specificity and sensitivity, Ready-to-use reagents
Function Detection of progesterone levels in serum/plasma
Portable No
Color White/Blue (Box)
Wall Mounted No
Power Source Other
Material Other
Measurement Range Up to the analytical range specified in the IFU
Equipment Type Chemiluminescence Immunoassay (CLIA) Kit
Condition New
Operating Type Automatic
Use Quantitative determination of Progesterone in human serum or plasma

Intended User For professional in-vitro diagnostic use only
Test Principle Sandwich Chemiluminescence Immunoassay
Lot Number Labeled on the kit
Internal Control Included in Kit
Pack Size Each kit contains all necessary reagents for specified number of tests
Barcode Available on packaging
Instructions for Use Detailed IFU provided in the kit
Expiry Date Labeled on the box
Calibration Calibration required as per instrument protocol
Sample Type Human serum or plasma

Product Description

Brand	Mindray
Sample Type	Serum
Pack Size	2 x 50T, 2 x 100T
CAT No.	10500422800, 10500425500

Mindray Progesterone (P4) is a CLIA-based in-vitro diagnostic immunoassay reagent for the quantitative determination of progesterone in human serum. Designed for compatible Mindray automated chemiluminescence immunoassay analyzers, it supports reproductive hormone testing, ovulation assessment, luteal function evaluation, fertility investigations, and endocrine laboratory diagnostics.

Advanced CLIA Technology for Accurate Results

Harnessing chemiluminescence immunoassay (CLIA) technology, the Mindray Progesterone kit enables highly sensitive and specific detection of progesterone in clinical samples. This quantitative method provides precise data essential for diagnostics, with built-in controls guaranteeing result reliability. Each ready-to-use kit is manufactured under stringent quality conditions, supporting robust laboratory workflows.

Seamless Integration and Ease of Use

The kit is tailored for Mindray CL-series analyzers, ensuring seamless integration into existing laboratory systems. Detailed instructions and barcode labeling simplify inventory and test setup, while automatic operation on compatible instruments helps minimize user intervention. All reagents are pre-measured and supplied in a convenient white/blue box, optimizing efficiency for clinical laboratories.

FAQ's of Mindray Progesterone (CLIA):

Q: How is the Mindray Progesterone (CLIA) test performed in the laboratory?

A: The test is carried out on compatible Mindray CL-series analyzers, using an automatic process based on the sandwich chemiluminescence immunoassay principle. Human serum or plasma samples are processed with the kit's pre-dispensed reagents as described in the included Instruction for Use (IFU).

Q: What samples are suitable for the Mindray Progesterone (CLIA) kit?

A: This kit is designed for use with human serum or plasma samples. It is intended for professional in-vitro diagnostic application within clinical or laboratory settings.

Q: When should the calibration and controls be performed during testing?

A: Calibration should be performed according to your instrument's protocol as outlined in the IFU. Internal controls are included in the kit and should be run as specified to ensure the accuracy and validity of test results.

Q: Where can I find critical information like expiry dates and lot numbers?

A: The expiry date is labeled directly on the outside of the kit box, while the lot number is indicated on the kit's packaging. For added traceability, a barcode is also present on the packaging.

Q: What are the storage requirements for the Mindray Progesterone (CLIA) kit?

A: The kit must be stored at 2-8C and should not be frozen. Always refer to the box for the stated expiration date, which is typically 12-18 months from the date of manufacture.

Q: What are the key benefits of using this kit in the laboratory?

A: This kit provides high specificity and sensitivity through advanced CLIA technology. It features ready-to-use reagents, integrated controls, and supports automated, real-time operation when used on Mindray CL-series analyzers, ensuring precise and efficient workflow in diagnostic settings.

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