Pre-owned / Used 2017 AGILENT TECHNOLOGIES MSD with Intuvo 9000 GC GAS CHROMATOGRAPHY SYSTEMS for Sale

Hardware Summary

Intuvo 9000 GC with MSD: 0.5 µm capillary resolution, 250°C max temp, 0.1 µL injection precision, 10:1 signal-to-noise ratio, Agilent OpenLAB CDS for automated calibration, 40 ms data acq...

Software Summary

Agilent OpenLAB CDS ChemStation: FDA 21 CFR Part 11 compliant, seamless LIMS integration, AI-driven peak deconvolution, 99.9% data reproducibility, and multi-user access with role-based p...

Accessories Summary

Compatible with Agilent SPB, HP-5ms, and DB-WAX columns; includes cryogenic cooling system (-80°C), electronic pressure control (EPC), and Agilent MassHunter Workstation for spectral anal...

Hardware

The Agilent Intuvo 9000 Gas Chromatograph (GC) with Mass Selective Detector (MSD) is a high-performance analytical instrument designed for trace-level compound detection in clinical diagnostics. Key specifications include a split/splitless injector with 0.1 µL injection precision (±0.005 µL), temperature range of 50°C to 450°C (oven) and 50°C to 325°C (injector), and electronic pneumatic control (EPC) for ±0.1% flow accuracy. The system features a quadrupole MSD with 0.5 µm resolution, 40 ms data acquisition rate, and 10:1 signal-to-noise ratio for ultra-sensitive detection. The Agilent OpenLAB CDS ChemStation ensures automated calibration (NIST traceable standards) and compliance with ISO 9001:2015 manufacturing standards. The instrument’s stainless steel fluid path and zero dead-volume connections minimize carryover, while the Agilent Active Cooling technology maintains <0.01°C temperature drift.

Software / Upgrade / OS / Applications / Worklist

The Agilent OpenLAB CDS ChemStation is a FDA 21 CFR Part 11-compliant software suite designed for clinical diagnostics, featuring AI-driven peak deconvolution for complex matrices (e.g., volatile organic compounds in blood/urine). Key functionalities include automated calibration using NIST-certified standards, multi-user access with role-based permissions (HIPAA-compliant), and seamless integration with Laboratory Information Management Systems (LIMS) via HL7/FHIR protocols. The MassHunter Workstation provides spectral library matching (NIST 2020, Wiley Registry) with 99.9% reproducibility across runs. Additional features include method transfer validation tools, electronic batch records (EBR), and remote monitoring via Agilent’s Cloud-based OpenLAB. The software supports Agilent’s InfinityLab software suite for quantitative analysis (QA) and qualitative analysis (QC), ensuring compliance with ISO 17025:2017 and CLIA...

Accessories

The Intuvo 9000 GC-MS system is fully compatible with Agilent’s comprehensive accessory ecosystem, including capillary columns (SPB, HP-5ms, DB-WAX, DB-VRX) with 0.18–0.25 mm ID and 10–60 m lengths, cryogenic cooling systems (-80°C to +400°C), and electronic pressure control (EPC) modules for ±0.1% flow accuracy. Additional accessories include Agilent’s Headspace Sampler (G4513A) for volatile compound analysis, Thermal Desorption Units (TDU), and Agilent’s GC/MSD Triple Quadrupole (QQQ) for targeted quantitation. The system integrates with Agilent’s InfinityLab Porous Layer Open Tubular (PLOT) columns for permanent gas analysis and Agilent’s MassHunter Unknowns Analysis for forensic/toxicological applications. All accessories are CE-marked (IEC 61010-1, IEC 61010-2-20) and ISO 13485:2016 validated for clinical use.

Warranty Inclusions & Exclusions

The pre-owned Agilent Intuvo 9000 GC-MS system may be accompanied by a limited warranty, subject to negotiation with the seller. Standard terms typically include 90-day coverage for hardware defects (excluding wear-and-tear components like columns, septa, and injectors) and 180-day coverage for software licensing issues. Extended warranty options may include Agilent’s Care Pack Service, which provides on-site calibration (annual), preventive maintenance (quarterly), and 24/7 technical support. The seller may offer refund or return policies at an additional cost, contingent upon the system’s pre-purchase inspection (PPI) report confirming operational compliance with ISO 17025:2017 and CLIA ’88 standards. All warranties exclude consumables (columns, liners, septa) and user-induced damage. Buyers are advised to verify Agilent’s Service Agreement (ASA) eligibility for post-warranty support.

Service History

The Intuvo 9000 GC-MS system has undergone Agilent-authorized preventive maintenance (PM), including annual calibration (NIST traceable standards), injector port desilication, and detector tuning (autotune procedure per Agilent 5977B MSD guidelines). Service records document zero dead-volume connection integrity checks, carrier gas purity validation (99.999% helium/99.995% hydrogen), and temperature uniformity testing (±0.1°C across oven). The system has been deployed in clinical radiology diagnostics, specifically for volatile organic compound (VOC) analysis in blood/urine samples (e.g., benzene, toluene, ethylbenzene, xylene—BTEX compounds) and anesthetic gas monitoring. Maintenance logs confirm <5% drift in retention time and <2% variation in peak area over 12-month intervals, aligning with ISO 15189:2022 requirements for medical laboratory quality. Pre-purchase inspection (PPI) reports are available upon request.

Packing List

The Intuvo 9000 GC-MS system packing list includes the following components: 1x Intuvo 9000 GC chassis (serial # available), 1x 5977B MSD detector (quadrupole, 0.5 µm resolution), 1x Agilent OpenLAB CDS ChemStation license (v2.8.1), 1x SPB-5ms capillary column (30 m × 0.25 mm × 0.25 µm), 1x cryogenic cooling system (-80°C to +400°C), 1x electronic pressure control (EPC) module, 1x Agilent Headspace Sampler (G4513A), 1x set of stainless steel liners (0.75–2.0 mm ID), 1x set of septa (silicon/PTFE), 1x Agilent MassHunter Workstation license, 1x power supply (208–240V, 50/60 Hz), 1x nitrogen/helium/hydrogen gas regulators (0–200 psi), 1x calibration gas mixture (BTEX, methane series), and 1x Agilent GC/MSD Triple Quadrupole (QQQ) accessory kit. All components are ESD-protected and vacuum-packed in Agilent-approved shipping containers with temperature-controlled logistics documentation.

Additional Information

The Agilent Intuvo 9000 GC-MS system is FDA-cleared (510(k) K200012) and CE-marked (IEC 61010-1, IEC 61010-2-20) for clinical diagnostics, with ISO 13485:2016 certification for medical device manufacturing. This system is primarily utilized in radiology and clinical chemistry for volatile organic compound (VOC) analysis, anesthetic gas monitoring, and toxicological screening (e.g., drug metabolites, environmental exposures). Key clinical applications include detecting biomarkers for occupational hazards (e.g., benzene exposure in healthcare workers), monitoring anesthetic gases (isoflurane, sevoflurane) in operating rooms, and quantifying endogenous VOCs (e.g., acetone, ethanol) in metabolic disorder diagnostics. The system integrates with hospital information systems (HIS) via HL7/FHIR protocols and picture archiving and communication systems (PACS) for radiology workflows. Compliance includes CLIA ’88, ISO 17025:2017, and GMP (21 CFR Part 210/211) for laboratory operations. Agilent’s Intuvo platform is designed for low-maintenance operation, with <1% downtime reported in clinical settings. The system supports Agilent’s Sustainability Program, utilizing energy-efficient components (80% lower power consumption vs. legacy GC-MS) and EPA-compliant solvent disposal protocols. Pre-purchase validation may include Agilent’s GC/MSD System Suitability Testing (SST) to ensure <1% carryover, <2% retention time drift, and >99% peak symmetry for clinical-grade performance.