Refurbished Triple Quadrupole LC / MS System Ultivo CLIA Non-Waived

Features

• Certified Pre-Owned Ultivo Triple Quadrupole LC / MS - Includes G6465B analytical HW, PC, install, intro 1Y SW upgrade/phone assist
• Ultivo is a compact, stackable triple quadrupole LC/MS/MS that eliminates the MS footprint by incorporating the mass spectrometer into the HPLC stack
• Representing a transformative approach to triple quadrupole mass spectrometry, Ultivo provides the fit-for-purpose, straightforward, and rugged LC/MS analysis you expect from larger comparable systems, but at a fraction of their size
• Multiple ion source configurations available, including Agilent Jet Stream and traditional ESI
• VacShield eliminates the need to vent the system while performing ion injector maintenance, minimizing maintenance downtime and increasing laboratory efficiency
• Cyclone ion guide compresses the ion beam without loss of signal, resulting in higher ion transmission efficiencies and enhanced data quality
• Vortex collision cell provides efficient dissociation of ions in the cell, improved focusing and transmission of ions, and rapid clearance of the cell between mass transitions, thereby allowing for more MRMs/sec, zero crosstalk, and greater confidence in results by removing noisy background
• Vortex collision cell provides efficient dissociation of ions in the cell, improved focusing and transmission of ions, and rapid clearance of the cell between mass transitions, thereby allowing for more MRMs/sec, zero crosstalk, and greater confidence in results by removing noisy background
• Intuitive 'Quant-My-Way' software and the MassHunter Productivity App boost productivity by up to 40%, require less need for operator training, reduce time spent reviewing data, and simplify report generation
• Enhanced maintenance feedback (EMF) features deliver smart, self-aware diagnostics to ensure optimum uptime and help drive down maintenance costs
• Built-in technical controls combined with procedural controls ensure the security of your data, control access, and facilitate compliance as defined by US FDA 21 CFR Part 11, EU Annex 11 and similar national electronic record regulations