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OptiQnt™ Clinical Chemistry Kits

Certificates:ISO 9001:2015ISO 13485:2016ISO 14001:2015cGMP
NEXTGEN IN-VITRO DIAGNOSTICS PRIVATE LIMITEDSouth Delhi, DL
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Anchored to the MCA registerCIN U33110DL2015PTC279481
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  • OEM (your brand on our product)
Key attributesAll specs
Category
Clinical Chemistry Kits
Place of origin
South Delhi, DL, India

Highlights at a glance

  • Category: Clinical Chemistry Kits
  • Made in South Delhi, DL, India
  • Certified: ISO 9001:2015, ISO 13485:2016, ISO 14001:2015

Description

The clinical chemistry range offers reagents and assays for the quantitative analysis of biochemical markers in bodily fluids.

General Specifications

Product Type: Ready-to-use liquid clinical chemistry reagents Intended Use: Quantitative determination of routine biochemical parameters in human serum, plasma or urine, using semi-automated and fully automated clinical chemistry analysers

General Characteristics

Format: Liquid stable, ready-to-use reagents Methodology: Colorimetric/enzymatic/kinetic (parameter dependent) Instrument Compatibility: Open system; suitable for all major semi-automated and automated clinical chemistry analysers Specimen Type: Serum, plasma urine (parameter dependent) Assay Principle: Enzyme-substrate reaction with spectrophotometric endpoint measurement Measuring Wavelength: 340–750 nm (depending on parameter) Linearity Range: Broad linearity with reduced need for repeat dilutions (parameter specific, e.g., glucose up to 500 mg/dl) Stability: - Unopened vial: 14–24 months at 2–8°C - Opened vial: Typically 30–60 days at 2–8°C (parameter dependent) Packaging Sizes: 2 × 50 ml, 4 × 50 ml, 2 × 100 ml, 4 × 100 ml, 10 × 100 ml (customised pack sizes available) Controls and Calibrators: Compatible with NGIVD’s multi-parameter controls and calibrators

Performance Characteristics

Precision: CV% ≤5% intra- and inter-assay variation Accuracy: Correlation ≥0.98 with reference/gold-standard methods Sensitivity: Optimised detection limits to cover clinical decision ranges Interference: Minimal effect from hemolysis, icterus, or lipemia (verified per) Reagent Blank: Provided where applicable

Trade & shipping terms

Set by NEXTGEN IN-VITRO DIAGNOSTICS PRIVATE LIMITED — the supplier's own terms.

CustomisationOEM Available

Certificates

ISO 9001:2015
ISO 13485:2016
ISO 14001:2015
cGMP

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NEXTGEN IN-VITRO DIAGNOSTICS PRIVATE LIMITED
Unverified<1 yr on BharatSealSouth Delhi, Delhi
Year founded
2015
Certifications
4

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