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Thermo Scientific Finnpipette F1 Adjustable-Volume Pipette

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Brand Thermo Fisher
Origin USA
Model Finnpipette F1 Adjustable-Volume Pipette
Sterilization Ag⁺ ion antimicrobial surface treatment
Volume Adjustment Mechanism Set-and-forget locking dial
Tip Ejection Low-force tactile ejection
Ergonomic Design 120° adjustable finger rest
Precision Feature Super-blow-out piston for volumes ≤50 µL
Operating Principle Air displacement pipetting
Compliance Designed to meet ISO 8655 requirements for volumetric accuracy and repeatability

Overview

The Thermo Scientific Finnpipette F1 Adjustable-Volume Pipette is an engineered solution for high-frequency, precision liquid handling in regulated and research-intensive laboratory environments. Based on the air displacement principle, it delivers accurate and reproducible volume delivery across its full adjustable range—designed to conform to ISO 8655 standards for gravimetric performance, including accuracy (±0.5–2.5% depending on volume), repeatability (CV ≤0.2–0.6%), and linearity. Its robust polypropylene housing, combined with a metal-plated internal mechanism, ensures long-term mechanical stability under routine use. The pipette is calibrated at the factory using traceable reference standards and supports user verification and adjustment via standardized procedures compliant with GLP and ISO/IEC 17025 frameworks.

Key Features

  • Set-and-forget volume lock: A dedicated rotary dial with tactile feedback and mechanical lock prevents accidental volume changes during operation—critical for multi-step protocols or shared-instrument workflows.
  • Ag⁺ ion antimicrobial surface treatment: Integrated silver-ion technology inhibits microbial colonization on frequently contacted surfaces (barrel, plunger, tip ejector), reducing bioburden accumulation and supporting contamination control in cell culture, molecular biology, and diagnostic labs.
  • 120° adjustable finger rest: Ergonomically repositionable to accommodate diverse hand sizes and pipetting postures—reducing repetitive strain injury (RSI) risk during extended sessions involving hundreds of pipetting cycles per day.
  • Super-blow-out piston design: Optimized for volumes ≤50 µL, this feature ensures complete expulsion of low-surface-tension liquids (e.g., ethanol, DMSO, PCR master mixes) by extending piston travel beyond standard stroke limits—minimizing residual droplet retention.
  • Tactile low-force tip ejection: Requires ≤1.5 N actuation force, significantly below industry averages, mitigating thumb fatigue and enabling consistent tip seating and release—even when wearing gloves or performing rapid serial dilutions.
  • Smooth, linear plunger action: Dual-stage spring mechanism provides controlled aspiration and dispensing resistance, enhancing operator control and improving inter-user reproducibility in training-sensitive environments.

Sample Compatibility & Compliance

The Finnpipette F1 is compatible with universal conical-tip pipette tips meeting ISO 8655-2 dimensional specifications—including filtered and low-retention variants. It supports aqueous solutions, buffers, organic solvents (e.g., 70% ethanol, acetone), and viscous reagents up to 50% glycerol concentration. All models undergo rigorous leak testing and are certified to comply with ISO 8655 Parts 1–6 for metrological performance. Documentation packages include calibration certificates traceable to NIST standards, supporting audit readiness for FDA 21 CFR Part 11–governed workflows where electronic records and signature integrity apply. Routine maintenance aligns with manufacturer-recommended intervals (every 6–12 months) and can be performed in-house using authorized service kits.

Software & Data Management

While the Finnpipette F1 is a manual, non-electronic pipette, its design integrates seamlessly into digital lab ecosystems. Each unit carries a unique serial number engraved on the barrel for asset tracking in LIMS or CMMS platforms. Calibration logs, maintenance history, and user verification data can be recorded using Thermo Fisher’s free LabTrack™ template suite—structured to support ALCOA+ data integrity principles (Attributable, Legible, Contemporaneous, Original, Accurate, Complete, Consistent, Enduring, Available). For labs implementing electronic quality management systems (eQMS), the pipette’s compliance with ISO/IEC 17025 clause 6.4.10 (equipment identification and status control) facilitates automated instrument status flagging and scheduled recalibration alerts.

Applications

This pipette is routinely deployed in applications demanding high volumetric fidelity and ergonomic sustainability: quantitative PCR setup, ELISA plate loading, cell suspension preparation, sample aliquoting for LC-MS analysis, and reagent dispensing in clinical chemistry analyzers. Its antimicrobial surface makes it especially suitable for BSL-2 microbiology labs and sterile tissue culture facilities. The super-blow-out function is validated for use with RNA extraction kits and single-cell sequencing library prep workflows where sub-microliter carryover directly impacts downstream assay sensitivity.

FAQ

Is the Finnpipette F1 autoclavable?
No—this model is not designed for autoclaving. Sterilization is limited to surface disinfection using 70% ethanol or isopropanol. Internal components are not heat- or steam-resistant.
Can I adjust the volume while the pipette is locked?
No—the set-and-forget dial must be manually unlocked before any volume change. This prevents unintentional drift during benchtop transport or multi-user shifts.
Does Thermo Fisher provide calibration services for this pipette?
Yes—certified calibration services are available globally through Thermo Fisher Service Centers, including ISO/IEC 17025-accredited reports with uncertainty budgets and as-found/as-left data.
What tip brands are compatible with the Finnpipette F1?
All tips conforming to ISO 8655-2 geometry for adjustable-volume pipettes (e.g., Thermo Fisher Finntips, Eppendorf Research plus tips, VWR Performance, and Rainin LTS tips) ensure optimal sealing and dispensing performance.
How often should I verify pipette performance?
Daily verification is recommended for critical applications (e.g., clinical diagnostics); weekly verification suffices for routine research use. Verification frequency should be defined in your lab’s SOPs based on risk assessment per ISO/IEC 17025 clause 7.7.

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