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Thermo Scientific Maxi Mix II Vortex Mixer

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Brand Thermo Fisher Scientific
Origin USA
Manufacturer Thermo Fisher Scientific
Product Type Imported Laboratory Equipment
Model Maxi Mix II Vortex Mixer
Speed Range 100–3000 rpm
Platform Options 8.9 cm rubber pad platform & 2.5 cm cup-style platform
Dimensions (W×D×H) 11.4 × 15.2 × 17.7 cm
Power Supply 230 V, 50 Hz
Net Weight 3.6 kg
Operating Modes Continuous & Touch-Activated (Pulse)
Sample Hold 1–4 tubes or sealed conical flasks

Overview

The Thermo Scientific Maxi Mix II Vortex Mixer is a robust, benchtop vortexing instrument engineered for reproducible and high-efficiency mixing of liquid samples in research, clinical, and quality control laboratories. It operates on the principle of orbital eccentric motion—generating rapid circular agitation through an off-center drive shaft—to induce homogeneous suspension, resuspension, or emulsification of viscous or particulate-laden solutions. Designed for routine sample preparation workflows—including bacterial suspension standardization, solvent-based extraction, reagent reconstitution, and cell lysis buffer homogenization—the Maxi Mix II delivers consistent shear energy across variable sample volumes and container geometries without requiring manual intervention or repeated tube tapping.

Key Features

  • Two interchangeable platforms: a 8.9 cm diameter soft rubber pad optimized for simultaneous vortexing of up to four test tubes or sealed conical flasks (e.g., 125 mL Erlenmeyer), and a compact 2.5 cm cup-style platform for precise single-tube mixing with enhanced stability at high speeds;
  • Adjustable speed control (100–3000 rpm) via calibrated rotary dial, enabling fine-tuned optimization for low-viscosity buffers or high-density suspensions;
  • Dual operating modes—continuous mode for extended mixing cycles and touch-activated pulse mode for controlled, momentary agitation ideal for temperature-sensitive or foaming-prone samples;
  • Heavy-duty cast metal base integrated with vacuum suction cups ensures vibration-dampened operation even during prolonged use at maximum speed;
  • Ergonomic design with low-profile footprint (11.4 × 15.2 × 17.7 cm) and lightweight construction (3.6 kg) facilitates integration into crowded fume hoods, biosafety cabinets, or cold room environments;
  • Compliance-ready engineering: CE-marked, RoHS-compliant, and designed to support GLP/GMP-aligned documentation practices through consistent mechanical performance and traceable operational parameters.

Sample Compatibility & Compliance

The Maxi Mix II accommodates a broad range of standard laboratory vessels including 0.5–50 mL microcentrifuge tubes, 13–17 mm round-bottom culture tubes, and sealed conical flasks up to 125 mL. Its soft, non-slip rubber platforms minimize tube slippage and prevent cap loosening during vigorous agitation. The device is routinely deployed in applications governed by ASTM D2709 (water separation in fuel emulsions), USP (dissolution testing auxiliary mixing), and ISO 8573-7 (aerosol generation for particle challenge studies). While not inherently 21 CFR Part 11 compliant as a standalone hardware unit, its consistent mechanical output supports audit-trail integrity when paired with validated lab information management systems (LIMS) or electronic lab notebooks (ELN).

Software & Data Management

As a purely electromechanical vortex mixer, the Maxi Mix II does not incorporate embedded firmware, digital displays, or connectivity interfaces. All operational parameters—including speed setting, mode selection, and runtime—are manually controlled and user-determined. This analog architecture eliminates software validation requirements and ensures long-term reliability under continuous duty cycles. For laboratories implementing computerized system validation (CSV), the absence of programmable logic or data logging simplifies qualification protocols (IQ/OQ/PQ) and reduces maintenance overhead associated with firmware updates or cybersecurity assessments.

Applications

  • Microbiological sample preparation: uniform resuspension of lyophilized cultures or colony-forming unit (CFU) standardization prior to plating or spectrophotometric quantification;
  • Pharmaceutical QC: dissolution media conditioning, excipient dispersion, and active pharmaceutical ingredient (API) suspension homogeneity verification;
  • Molecular biology: lysis buffer mixing prior to DNA/RNA extraction, protein solubilization, and antibody conjugation reactions;
  • Clinical diagnostics: whole blood or serum homogenization for immunoassay calibration standards and proficiency testing panels;
  • Environmental testing: extraction of analytes from solid-phase matrices using organic solvents, followed by phase separation and supernatant recovery.

FAQ

Is the Maxi Mix II suitable for use with hazardous or volatile solvents?
Yes—its fully enclosed motor housing and non-sparking drive mechanism meet general laboratory safety standards for use with common organic solvents; however, operation within explosion-proof enclosures is recommended for Class I, Division 1 environments.
Can the Maxi Mix II be used inside a refrigerated chamber or cold room?
Yes—the device operates reliably at ambient temperatures ranging from 4 °C to 40 °C and maintains consistent torque output across this range; condensation on external surfaces should be minimized via proper acclimatization before power-on.
Does Thermo Fisher provide calibration certificates or performance verification protocols?
No factory-issued calibration certificate is supplied, but users may perform speed verification using a handheld tachometer; Thermo Fisher Technical Support provides documented OQ test procedures upon request for GxP-regulated environments.
What maintenance is required for long-term reliability?
Routine cleaning of the rubber platforms with 70% ethanol and periodic inspection of suction cup adhesion are sufficient; no lubrication or internal servicing is required under normal operating conditions.

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