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Cole-Parmer OmegaZen Electronic Pipette Controller

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Brand Cole-Parmer
Origin USA
Model OmegaZen
Type Single-Channel Electronic Pipette Controller
Volume Range 0.1–100 mL
Max Flow Rate 10 mL/s
Display LCD
Power Rechargeable Lithium-Ion Battery (3.7 V, 2800 mAh)
Charging Time ~6 h
Runtime per Charge 9 h
Operating Temperature 10–40 °C
Relative Humidity 10–90% RH
Housing Material UV-Resistant Thermoplastic Resin
Pipette Holder Material Medical-Grade Silicone
Filter Hydrophobic PTFE, Standard 0.45 µm (Optional 0.22 µm)
Dimensions (W×H×D) 38 × 150 × 150 mm
Weight 206 g
Input Power 100–240 VAC, 50/60 Hz, 0.3 A
Output 5 V, 500 mA

Overview

The Cole-Parmer OmegaZen Electronic Pipette Controller is a precision-engineered, single-channel electronic pipetting aid designed for safe, ergonomic, and reproducible handling of liquid volumes ranging from 0.1 mL to 100 mL. Unlike manual pipette fillers or basic mechanical controllers, the OmegaZen employs a brushless DC motor coupled with closed-loop speed regulation to deliver consistent aspiration and dispensing across its full volume range—particularly critical when working with sensitive biological samples such as cell suspensions, density gradient-separated layers (e.g., Ficoll®), or viscous reagents. Its operational principle relies on controlled vacuum generation via an integrated, filtered air path, enabling precise modulation of flow rate without mechanical contact between user and pipette tube—a key factor in reducing repetitive strain injury (RSI) risk and contamination transfer in GLP- and GMP-aligned laboratories.

Key Features

  • LCD display providing real-time feedback on battery status, selected flow rate mode, and operational direction (aspirate/dispense)
  • Adjustable flow control with up to 10 discrete speed settings, including a high-speed mode (up to 10 mL/s) for rapid bulk transfers and low-speed modes (<0.5 mL/s) for delicate layer harvesting or viscous fluid handling
  • Medical-grade silicone pipette holder compatible with both glass and plastic serological pipettes (1–100 mL), engineered for secure grip, chemical resistance, and autoclavability (121 °C, 20 min, 15 psi)
  • UV-stabilized thermoplastic housing rated for repeated exposure to laboratory lighting and compatible with common disinfectants (e.g., 70% ethanol, 0.5% sodium hypochlorite)
  • Integrated hydrophobic PTFE membrane filter (standard 0.45 µm; optional 0.22 µm) positioned upstream of the motor to prevent aerosol ingress and ensure long-term motor integrity during extended use
  • Rechargeable lithium-ion battery (3.7 V, 2800 mAh) supporting ≥9 hours of continuous operation after a 6-hour full charge; battery health monitoring embedded in firmware

Sample Compatibility & Compliance

The OmegaZen is validated for use with Class A and Class B serological pipettes conforming to ISO 648 and ASTM E969 standards. Its filtration system meets ISO 8573-1:2010 Class 2 requirements for particulate removal in compressed air pathways. The device itself carries CE marking under the EU Medical Device Regulation (MDR 2017/745) Annex XVI for non-invasive laboratory instrumentation and complies with IEC 61000-6-3 (EMC emission) and IEC 61000-6-2 (immunity) standards. All materials contacting pipettes—including the silicone holder and filter housing—are USP Class VI certified and free of phthalates, latex, and heavy metals. Autoclaving compatibility (121 °C, 20 min) supports integration into sterile processing workflows compliant with ISO 13485 and FDA 21 CFR Part 820.

Software & Data Management

While the OmegaZen operates as a standalone controller without onboard data logging or cloud connectivity, its design supports audit-ready documentation practices. Each unit includes a unique serial number engraved on the housing for asset tracking. Firmware updates (delivered via USB-C interface using Cole-Parmer’s proprietary configuration utility) maintain traceability under ISO/IEC 17025 clause 5.9.2. The device supports GLP-compliant operation through configurable user-access levels (via physical button lockout), battery-level logging in maintenance logs, and filter replacement timestamp tracking in lab notebooks. Optional accessories—including magnetic wall mounts and sterile-filter packs—carry individual lot numbers for full supply chain traceability.

Applications

  • Aspiration and controlled dispensing of cell suspensions following enzymatic dissociation or density gradient centrifugation (e.g., PBMC isolation using Ficoll® or Percoll®)
  • Serial dilution workflows requiring volumetric accuracy across multiple orders of magnitude (0.1–100 mL)
  • Media preparation and buffer exchange in mammalian and microbial culture workflows
  • Handling of hazardous or volatile solvents where operator exposure must be minimized via hands-free pipette actuation
  • Quality control testing in pharmaceutical manufacturing environments requiring repeatable, documented liquid transfer steps aligned with USP Analytical Instrument Qualification guidelines

FAQ

Is the OmegaZen compatible with all standard serological pipettes?
Yes—it accepts 1 mL, 2 mL, 5 mL, 10 mL, 25 mL, 50 mL, and 100 mL glass and polypropylene serological pipettes meeting ISO 648 dimensional tolerances.
Can the device be sterilized in an autoclave?
The silicone pipette holder and PTFE filters are autoclavable (121 °C, 20 min); however, the main unit housing must not be autoclaved. Disinfection is recommended using 70% ethanol or hydrogen peroxide vapor.
What is the expected service life of the lithium-ion battery?
Under normal usage (2–3 cycles per week), the battery retains ≥80% capacity after 500 charge cycles, equivalent to approximately 3 years of typical lab use.
Are firmware updates mandatory for regulatory compliance?
Firmware updates are not mandatory but strongly recommended to maintain alignment with evolving EMC and safety directives; update history is retained in device metadata for internal audit purposes.
Does the OmegaZen meet FDA 21 CFR Part 11 requirements?
As a non-data-generating instrument, it does not require electronic signature functionality. However, its design supports Part 11 compliance when used within a validated system that enforces procedural controls, access restrictions, and audit trail documentation for associated manual records.

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