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Thermo Scientific Finnpipette F3 Adjustable-Volume Single-Channel Pipette

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Brand Thermo Fisher Scientific
Origin USA
Model F3-10 (1–10 µL)
Pipette Type Manual Single-Channel Adjustable-Volume Pipette
Volume Range 1–10 µL
Maximum Capacity 10 µL
Accuracy ±3.5% at 1 µL, ±1.0% at 10 µL
Precision (CV) ≤1.5% at 10 µL
Tip Compatibility Universal Finntip and ISO-standard conical tips
Ergonomic Features Dual-control plunger, color-coded volume display, wide thumb rest, soft-grip polymer housing
Blow-out Function Enhanced positive displacement blow-out for volumes ≤50 µL
Compliance ISO 8655-2:2022, EN ISO 13485 certified manufacturing

Overview

The Thermo Scientific™ Finnpipette™ F3 Adjustable-Volume Single-Channel Pipette is an ISO 8655-2:2022 compliant manual liquid handling instrument engineered for high reproducibility and operator comfort in routine and precision laboratory workflows. Designed using first-principles volumetric displacement mechanics, the F3 operates on air-cushion (positive displacement) principles—where piston movement within a sealed barrel displaces ambient air to aspirate and dispense liquid through a disposable tip. Its calibrated spring-loaded mechanism ensures consistent plunger resistance across the full 1–10 µL range, minimizing inter-operator variability and fatigue during repetitive pipetting tasks. The device is manufactured under an EN ISO 13485-certified quality management system, reflecting adherence to medical device-grade traceability and process control standards applicable to regulated environments including clinical diagnostics and pharmaceutical QC labs.

Key Features

  • Dual-control plunger system: Separate top rotation cap prevents accidental volume adjustment during operation; bottom plunger delivers precise stroke actuation with low force (<1.2 N at full stroke)
  • Ergovisio™ large-volume display: High-contrast, rotatable scale with color-coded volume bands (blue for 1–10 µL range) enables rapid visual verification without repositioning the hand
  • Wide, contoured thumb rest: Molded from soft-touch thermoplastic elastomer (TPE) with anatomical curvature to reduce median nerve pressure during extended use
  • Enhanced blow-out function: Optimized piston travel and tip ejection geometry ensure complete liquid expulsion for viscous or volatile samples at volumes ≤10 µL
  • Universal tip compatibility: Accepts all ISO 8655-compliant conical tips—including Thermo Finntip, Eppendorf, Gilson, and Rainin—verified via dimensional metrology per ISO 8655-5
  • Chemical-resistant housing: Polypropylene and POM (polyoxymethylene) construction withstands repeated exposure to 70% ethanol, 10% sodium hypochlorite, and common lab solvents

Sample Compatibility & Compliance

The F3-10 pipette supports accurate handling of aqueous buffers, cell suspensions, DNA/RNA solutions, serum, and low-viscosity organic solvents (e.g., acetonitrile, methanol). It is validated for use with standard low-retention and filtered tips rated for ≤10 µL applications. Regulatory alignment includes full traceability to NIST-traceable calibration standards, documented in factory calibration certificates supplied with each unit. The design conforms to ISO 8655 parts 1–7 for performance testing, metrological requirements, and uncertainty evaluation. In GLP/GMP environments, the pipette supports audit-ready documentation when paired with Thermo’s optional calibration logbook templates and user-defined maintenance schedules.

Software & Data Management

As a fully manual instrument, the F3-10 does not incorporate onboard electronics or digital connectivity. However, its mechanical architecture is optimized for integration into digitally managed workflows: volume settings are physically indexed and lockable, enabling unambiguous recording in electronic lab notebooks (ELNs) such as LabArchives or Benchling. Calibration records—including date, technician ID, reference standard used (e.g., gravimetric method per ISO 8655-6), and deviation results—can be archived in compliance with FDA 21 CFR Part 11 requirements when entered into validated LIMS or ELN platforms. Thermo provides downloadable PDF templates for calibration logs, preventive maintenance checklists, and user training sign-offs aligned with ISO/IEC 17025 clause 6.4.10.

Applications

  • Quantitative PCR (qPCR) setup requiring precise 1–10 µL template or master mix dispensing
  • High-throughput screening (HTS) assay plate preparation where inter-assay CV <2.0% is mandated
  • Cell culture passaging involving small-volume trypsin or media additions
  • Standards preparation for HPLC or LC-MS calibration curves
  • CRISPR guide RNA complex assembly with limiting reagent volumes
  • Microvolume spectrophotometry sample loading onto NanoDrop or similar platforms

FAQ

Is the F3-10 compatible with filter tips for sterile applications?

Yes—its tip cone geometry meets ISO 8655-5 dimensional tolerances for Class A filter tips rated down to 10 µL. Sterility validation data is available upon request.
What is the recommended recalibration interval under ISO 8655 guidelines?

Annual calibration is advised for routine use; however, laboratories operating under GxP must perform interval verification based on risk assessment—typically every 3–6 months for critical assays.
Can the F3-10 be autoclaved?

No—the internal spring and O-ring materials are not autoclave-rated. Surface decontamination with 70% ethanol or 10% bleach is permitted.
Does Thermo provide certified calibration services for this model?

Yes—accredited third-party calibration services (ISO/IEC 17025) and in-house Thermo-certified calibration kits with NIST-traceable weights are available globally.
How does the dual-control plunger improve pipetting accuracy?

By decoupling volume setting (top cap) from aspiration/dispense action (bottom plunger), it eliminates unintended volume drift caused by lateral thumb pressure during repeated operation—a documented source of systematic error per ISO/TR 20692.

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