IKA VORTEX 1 Compact Vortex Mixer
| Brand | IKA |
|---|---|
| Origin | Germany |
| Manufacturer | IKA-Werke GmbH & Co. KG |
| Model | VORTEX 1 |
| Oscillation Frequency | 1000–2800 rpm |
| Oscillation Amplitude | 4.5 mm |
| Maximum Tube Diameter | 30 mm |
| Drive Type | Circular Orbit |
| Motor Input Power | 1.2 W |
| Motor Output Power | 0.8 W |
| Continuous Duty Cycle | 100% |
| Operating Temperature Range | 5–40 °C |
| Relative Humidity Limit | ≤80% (non-condensing) |
| Ingress Protection Rating | IP40 |
| Voltage | 100–240 V AC, 50/60 Hz |
| Device Weight | 0.828 kg |
| Dimensions (W × D × H) | 95 × 70 × 110 mm |
| Housing Material | Chemical-resistant polymer |
| Base Material | Zinc alloy with protective coating |
| Touch-activated Pulse Mode | Yes |
| Speed Display | None |
| Timer Function | None |
Overview
The IKA VORTEX 1 is a compact, benchtop vortex mixer engineered for rapid, reproducible homogenization of small-volume liquid samples in standard laboratory tubes. Operating on the principle of circular orbital motion—where the sample platform rotates eccentrically at a fixed amplitude of 4.5 mm—the device generates controlled shear forces that efficiently suspend, resuspend, or mix viscous or particulate-laden solutions. Designed for routine use in molecular biology, clinical diagnostics, and pharmaceutical quality control labs, the VORTEX 1 delivers consistent mixing performance without thermal input or mechanical complexity. Its brushless motor architecture ensures long-term operational stability, low electromagnetic interference, and minimal maintenance requirements—critical attributes for GLP-compliant environments where equipment traceability and functional consistency are auditable parameters.
Key Features
- Adjustable speed range from 1000 to 2800 rpm, enabling optimization across diverse sample viscosities and container types (e.g., 0.2–15 mL Eppendorf tubes, microcentrifuge tubes, and standard test tubes up to 30 mm diameter)
- Integrated touch-sensitive pulse activation for transient mixing—ideal for sensitive biological samples requiring brief, high-intensity agitation without prolonged exposure to shear stress
- Chemical-resistant polymer housing and coated zinc alloy base provide structural rigidity, corrosion resistance, and vibration damping under continuous operation
- IP40-rated enclosure meets IEC 60529 standards for protection against solid objects ≥1 mm, supporting safe deployment in shared lab spaces with variable ambient conditions
- Universal power supply (100–240 V AC, 50/60 Hz) enables seamless integration into international laboratory infrastructure without voltage conversion hardware
- Compact footprint (95 × 70 × 110 mm) and low mass (0.828 kg) allow flexible placement on biosafety cabinets, cold room benches, or automated workstation peripheries
Sample Compatibility & Compliance
The VORTEX 1 accommodates common single-use and reusable tube formats used in nucleic acid extraction, ELISA preparation, reagent reconstitution, and cell suspension protocols. It supports conical-bottom and round-bottom tubes with diameters up to 30 mm and nominal volumes between 0.2 mL and 15 mL. No heating or cooling elements are integrated; therefore, it complies with ISO 13485 Annex C requirements for non-active medical device accessories and satisfies essential safety clauses under EN 61010-1:2010 for electrical equipment used in laboratory environments. While not equipped with electronic audit trails or time-stamped event logging, its mechanical simplicity aligns with FDA 21 CFR Part 11 risk-based validation strategies when deployed as a secondary mixing tool within documented SOPs.
Software & Data Management
The IKA VORTEX 1 operates as a standalone analog instrument with no embedded microcontroller, firmware, or digital interface. Consequently, it does not support USB connectivity, remote control, or data export functionality. All operational parameters—including speed selection and pulse activation—are executed manually via capacitive touch sensing. This design eliminates software-related validation burdens, reduces cybersecurity surface area, and simplifies IQ/OQ documentation for regulated laboratories. Users may incorporate the device into broader electronic lab notebook (ELN) workflows by referencing its model-specific technical specifications (e.g., IKA Doc. No. 30012788) and maintaining calibration records per internal maintenance schedules.
Applications
- Rapid resuspension of lyophilized reagents and enzyme preparations prior to assay setup
- Homogenization of PCR master mixes containing Taq polymerase, dNTPs, and primers
- Uniform dispersion of magnetic beads during nucleic acid isolation workflows
- Pre-mixing of immunoassay diluents and conjugate solutions in clinical chemistry platforms
- Disaggregation of precipitated proteins or inclusion bodies in recombinant expression studies
- Standardized vortexing steps in USP <71> sterility test procedures and EP 2.6.27 microbial enumeration methods
FAQ
Does the VORTEX 1 include a timer or programmable dwell function?
No. The device lacks integrated timing circuitry and is intended for manual, operator-initiated operation only.
Can it be used with deep-well plates or multi-tube racks?
No. The platform is optimized for individual tube agitation; rack compatibility is not supported due to fixed orbital geometry and absence of universal clamping mechanisms.
Is speed calibration traceable to national standards?
While the unit does not ship with factory-issued calibration certificates, users may perform rotational speed verification using an external optical tachometer compliant with ISO/IEC 17025-accredited metrology practices.
What maintenance is required for long-term reliability?
Periodic inspection of the rubber damping feet and cleaning of the tube seat with 70% ethanol or isopropanol—avoiding chlorinated solvents—is recommended. No lubrication or internal servicing is specified by IKA.
Is the VORTEX 1 suitable for GMP manufacturing environments?
Yes—as a Class I, non-thermoregulated, non-data-generating auxiliary device, it may be qualified under Annex 15 guidelines when included in equipment master files and subjected to periodic functional checks.

