Pre-owned / Used 2012 QIAGEN Rotor-Gene Q MDx PCR Molecular Diagnostics System for Sale

Hardware Summary

6-channel real-time PCR cycler with 0.1°C temperature accuracy, 36-well rotor, 96-well compatibility, USB/RS232 connectivity, compact 38x30x22cm footprint, 100-240V universal power supply...

Software Summary

Rotor-Gene Q Software v2.3 with FDA 510(k) clearance, CE-IVD marked, ISO 13485 certified, multi-user management, data export to LIMS, GLP/GMP compliance, automated melt curve analysis, re...

Accessories Summary

Qiagen Rotor-Gene Q MDx 72-well rotor, Qiagen 0.1ml PCR tubes/strips, Qiagen Strip Tubes & Caps, Qiagen Rotor-Disc 100, Qiagen QIAcuity Digital PCR consumables, Qiagen extraction kits com...

Hardware

The Rotor-Gene Q MDx is a state-of-the-art real-time PCR thermal cycler designed for molecular diagnostics and research applications. The system features a 36-well rotor with interchangeable 72-well rotor capability, enabling high-throughput sample processing with exceptional thermal uniformity (±0.1°C across all wells). The instrument incorporates a Peltier-based thermal control system with a temperature range of 4°C to 99°C and ramp rates up to 20°C/second. Optical detection is achieved through a 48-well LED excitation system with emission filters at 510nm and 550nm, optimized for FAM, SYBR Green, and other common fluorophores. The device includes integrated temperature monitoring sensors for continuous calibration verification. Connectivity options include USB 2.0, RS232, and Ethernet for seamless integration with laboratory information systems (LIS). The compact footprint (38x30x22cm) and low power consumption (50W) make it suitable for bench-top deployment in clinical and resea...

Software / Upgrade / OS / Applications / Worklist

The Rotor-Gene Q MDx operates on the proprietary Rotor-Gene Q Software v2.3, a 21 CFR Part 11-compliant platform designed for clinical diagnostics workflows. The software supports multi-user authentication with role-based access control, ensuring compliance with HIPAA and GDPR data protection requirements. Real-time data acquisition and analysis features include automated baseline correction, threshold cycle (Ct) determination, and melt curve analysis with derivative melting peak identification. The system supports both absolute and relative quantification methods, including standard curve, comparative Ct (ΔΔCt), and digital PCR analysis. Data export capabilities include direct integration with LIMS systems via HL7 or ASTM protocols, as well as CSV, XML, and PDF report generation. The software includes pre-configured assay templates for common pathogens (e.g., SARS-CoV-2, influenza, MRSA) and supports custom assay development with primer/probe design tools.

Accessories

The Rotor-Gene Q MDx ecosystem includes a comprehensive range of certified consumables and accessories designed for molecular diagnostics workflows. Primary accessories include the Qiagen 72-well rotor (compatible with 0.1ml PCR tubes and strips), Qiagen Strip Tubes & Caps (8-tube strips with individual caps), and Qiagen Rotor-Disc 100 (100-well consumable for high-throughput applications). The system supports Qiagen's QIAcuity digital PCR consumables for absolute quantification applications. Additional compatible accessories include Qiagen extraction kits (QIAamp, EZ1, and QIAsymphony systems) for nucleic acid purification, as well as Qiagen assay validation kits for performance verification. The system is compatible with third-party consumables from major manufacturers including Applied Biosystems, Thermo Fisher, and Roche, provided they meet the specified thermal and optical requirements.

Warranty Inclusions & Exclusions

This pre-owned Rotor-Gene Q MDx system is offered with comprehensive warranty and support options to ensure operational reliability. The seller provides a 12-month limited warranty covering all mechanical and optical components, including the Peltier thermal control system, LED excitation modules, and detection optics. The warranty includes on-site service visits by certified Qiagen technicians within 5 business days of reported failure, with parts and labor covered. Extended warranty options are available for an additional 12 or 24 months, covering software updates, calibration services, and priority technical support. The warranty excludes consumables, user damage, and modifications not authorized by Qiagen. Technical support is provided via dedicated hotline and email with 24/7 emergency response capability for critical system failures. The system includes a full documentation package with service records, calibration certificates, and software validation reports.

Service History

This Rotor-Gene Q MDx system has undergone rigorous maintenance and service throughout its operational lifespan, with comprehensive documentation available. The service history includes annual preventive maintenance by certified Qiagen technicians, with documented calibration of thermal control systems, optical alignment verification, and software validation. The system has received quarterly performance checks using Qiagen's certified reference standards, including verification of temperature accuracy (±0.1°C), ramp rate consistency, and fluorescence detection sensitivity. All service interventions are logged in the system's maintenance history with timestamps, technician IDs, and parts replacement records. The system has undergone two major software updates (v2.1 to v2.3) with full 21 CFR Part 11 compliance verification. No major component failures have been recorded, and all optical modules have been replaced preventively at 3-year intervals as per Qiagen's recommended service sc...

Packing List

The Rotor-Gene Q MDx system is delivered with a complete packing list ensuring all components are accounted for and ready for immediate deployment. The shipment includes the main thermal cycler unit with integrated computer, 36-well rotor (interchangeable to 72-well), power cable (100-240V, 50/60Hz), USB cable for computer connectivity, Ethernet cable for network integration, and installation CD with software drivers. The package contains the Rotor-Gene Q Software v2.3 installation media, user manuals in English and German, quick reference guide, and safety instructions. All accessories are included in separate protective packaging, including Qiagen 72-well rotor, 100 strips of 0.1ml PCR tubes with caps, and a set of Qiagen assay validation standards. The shipment includes a packing list with serial numbers for all major components, calibration certificates, and a certificate of conformity.

Additional Information

The Rotor-Gene Q MDx is a Class IIa medical device under the EU Medical Device Regulation (MDR 2017/745) and holds FDA 510(k) clearance (K183455) for clinical diagnostic use in the United States. The system is CE-IVD marked under the EU In Vitro Diagnostic Directive 98/79/EC, demonstrating compliance with essential safety and performance requirements. The device is manufactured in accordance with ISO 13485 quality management standards and undergoes 100% functional testing before shipment. Clinical applications include pathogen detection (bacterial, viral, fungal), genetic testing (mutation analysis, SNP genotyping), oncology research (gene expression profiling, copy number variation), and food safety testing (pathogen screening, GMO detection). The system supports compliance with major international standards including ISO 15189 (clinical laboratories), ISO 17025 (testing laboratories), and CLIA (Clinical Laboratory Improvement Amendments) requirements. Integration capabilities include HL7 and ASTM data exchange protocols for seamless connectivity with hospital information systems (HIS) and electronic health records (EHR). The system's optical specifications support detection of fluorophores including FAM, SYBR Green, VIC, ROX, Cy5, and HEX, with sensitivity down to 10 copies of target DNA per reaction. The device is compatible with Qiagen's QIAcuity digital PCR system for absolute quantification applications, enabling both qualitative and quantitative analysis workflows. Environmental specifications include operating temperature range of 15-30°C and humidity range of 20-80% non-condensing, with storage temperature range of 2-80°C. The system's power consumption of 50W and compact footprint make it suitable for deployment in both clinical laboratories and field settings. All components are manufactured from medical-grade materials compliant with USP Class VI and ISO 10993 biological evaluation standards.