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The Ultimate
Electronic Bowie Dick Test

Ensure every autoclave cycle starts with confidence with SteriSense®

Reliable steam‑sterilization validation starts with a proven Air Removal - Steam Penetration Test. Ellab’s SteriSense® Electronic Bowie Dick Test delivers objective, real‑time proof that every autoclave cycle removes residual air and achieves full steam penetration, keeping you compliant and confident every day.

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The Industry Standard for Steam Sterilization Testing

The Bowie Dick Test is a required procedure for pre‑vacuum sterilizers according to GMP guidance. Residual air pockets can jeopardize sterilization quality and may result in audit issues. SteriSense® promptly detects air‑removal failures within around 60 seconds after the cycle, enabling proactive intervention before product loads are compromised.

Ensure the performance of your steam sterilizers with SteriSense®:

Prove complete air removal & steam penetration with objective electronic data.
Achieve daily compliance with FDA, EU‑GMP, ISO 17665 & 21 CFR Part 11.
Auto‑create tamper‑evident PDF reports in ValSuite®: No more manual paperwork.

Experience the Difference - Request Your Free Demo

Looking for reliable Bowie Dick Test solutions? Our experts can help. Fill out the form provided to explore Ellab’s sterilization validation products.

Unmatched Accuracy and Compliance

Our electronic Bowie Dick test stands out for its ultra-compact design, advanced analytics, and ease of use. The system is ISO 11140-4 compliant, supports up to 1,000 test cycles between calibrations, and provides detailed digital reports for audit readiness.

Ellab delivers reliable, objective, and fully traceable sterilization verification, minimizing downtime, maximizing compliance.

Key Features and Specs
  • ISO 11140-4:2007 type B1, B2, B3 compliant
  • For 121 °C and 134 °C steam sterilizers
  • Temperature range: 0 to +140 °C (calibrated +25 to +140 °C)
  • Temperature accuracy: ±0.05 °C
  • Pressure range: 10 mBar to 6 Bar
  • Pressure accuracy: ±0.25% Full Scale (±15 mBar)
  • Logger housing: 316L stainless steel
  • PCD housing: PEEK
  • Memory: 40.000 data points
  • Battery: up to 1,000 tests / 500 hours at +134 °C

Tailored Solutions for Every Sterilization Need

Ellab’s SteriSense® measures all critical sterilization parameters from temperature to pressure, and vacuum pulses, with high precision. The interchangeable Process Challenge Device (PCD) allows for multiple test cycles in sequence, minimizing downtime and resource use.

  • icon Chamber temperature (Pt1000 sensor)
  • icon PCD core temperature
  • icon Chamber pressure (piezoresistive sensor)
  • icon Vacuum pulse detection
  • icon Non-condensable gas (NCG) analysis
Purpose-Built Sensors for Reliable Steam Cycle Verification

SteriSense® goes beyond routine compliance: It's a powerful tool for continuous improvement. By capturing and storing granular sterilization data across cycles, departments can track trends, compare equipment performance, and preemptively identify deviations before they cause downtime.

Intuitive Software for Effortless Compliance

Ellab’s user-friendly ValSuite® software automates data collection, analysis, and reporting. It supports 21 CFR Part 11 compliance, generates objective pass/fail results, and provides secure, easily exportable reports for audits and quality assurance.

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Automated data transfer and analysis.
Objective, digital test results.
Secure, compliant data storage.
Customizable reporting and export options.
Visual cycle graphs and analytics.

A Global Partner for Compliance and Confidence

In regulated life science environments, compliance is the foundation of product safety, operational continuity, and patient trust. Ellab brings together equipment, expertise, and services to support your entire compliance life cycle. From commissioning and qualification to calibration and ongoing monitoring, we help you strengthen control, safeguard data integrity, and maintain consistent audit readiness across sites.

  • Specialized Knowledge: In-depth expertise in validation, monitoring, and calibration.
  • Global Presence: Local teams across 40+ countries, offering regional GMP and regulatory guidance.
  • Comprehensive Support: From accredited calibrations and rental services to SOP optimization and ongoing maintenance.
  • Trusted Collaboration: Partnering with leading pharma and biotech innovators to ensure compliance and audit-readiness.

Together, we build confidence through collaboration and compliance, every day, everywhere.

Take Your Processes to the Next Level

Ellab provides end-to-end solutions for process validation and monitoring, ensuring seamless integration and compliance across your sterilization lifecycle. Partner with us for comprehensive, audit-ready sterilization validation.