Portable Particle Counters – 3900 Series

Model 3905 3910 3920
Light Source Laser diode
Measuring Particle Size 0.3, 0.5, 1.0, 3.0, 5.0, 10.0 (μm) 0.5, 0.7, 1.0, 3.0, 5.0, 10.0 (μm)
Flow Rate 1.0 CFM (28.3 LPM) 1.77 CFM (50 LPM) 3.5 CFM (100 LPM)
Counting Efficiency 50±20% at 0.3μm 50±20% at 0.5μm
Concentration Limit 500,000 particles/ft³ at 10% coincidence loss 300,000 particles/ft³ at 10% coincidence loss
Sampling Time 6sec ~ 23hours 59min 59sec (configurable)
Interval Time 6sec ~ 23hours 59min 59sec (configurable)
Zero Count Level Less than 1 count / 5 minutes
Printer Built-in thermal printer
Display 6.4 inch color touch screen
Interface Ethernet, USB, Memory card slot (MMC)
Data Storage 10,000 data points
Security Password authentication and management, secure data, and audit trails (meets 21 CFR Part 11 compliance)
Reports ISO146441-1, GB/T16292-2010, FEDERAL STANDARD, BRITISH STANDARD, EU GMP
Standards ISO 21501-4, JIS B9921, CE
Power AC 100 – 240 V or Li-ion Battery
Dimensions W 7.9 x D 7.9 x H 8.1 inch
Weight 14.2 lbs (6.44 kg)
Warranty 2 year
Environmental Sensor Air Velocity, Temperature, Relative Humidity and Pressure
What’s included Quick-start guide, AC adapter, zero filter, Isokinetic probe with 79 inch (2m) tubing, inlet nozzle, data processing software, memory card, 2 rolls of cleanroom-grade printer paper, 1 x Li-ion battery and calibration certificate

Description

Portable Particle Counters – 3900 Series

High-Flow Airborne Particle Counters for Exact ISO Cleanroom Validation

Uncontrolled airborne contamination during pharmaceutical compounding, semiconductor packaging, or medical device assembly directly threatens yield and regulatory approval. Meeting modern sterilization standards requires a contamination diagnostic tool that is both highly mobile and completely precise.

The Kanomax 3900 Series Portable Particle Counters (featuring the high-performing Model 3910 and Model 3920) are the industry benchmark for facility-wide validation. Delivering up to 50 Liters Per Minute (LPM) sample flow rates, the 3900 Series drastically reduces testing windows by pulling large air volumes quickly. This ensures rapid, certified compliance verification across all structural zones.

 

Technical Performance & Operational Value

The 3900 Series eliminates operational downtime by combining an intuitive touchscreen interface with heavy-duty measurement standards.

Operational Feature System Specification Practical Cleanroom Advantage
High-Flow Sampling 28.3 LPM or 50.0 LPM flow options Captures a cubic meter of air quickly, speeding up routine verification cycles.
Multi-Channel Tracking 6 simultaneous size channels ($0.3\text{ to }10.0\,\mu\text{m}$) Monitors micro-contaminants and larger ambient macro-particles all at once.
Comprehensive Display Large, color touchscreen interface Allows technicians to navigate testing setups and map layouts without a PC.
Enclosure Materials Fully polished 304 stainless steel Resists aggressive chemical wipes and prevents cross-contamination.

Built to Withstand Strict Audits

1. Seamless Certification and Automation

  • Automated Cleanroom Standards: The onboard software automatically calculates and outputs pass/fail metrics based on ISO 14644-1, EU GMP Annex 1, and FS 209E requirements.

  • Airtight Data Security: Fully compatible with FDA 21 CFR Part 11 environments. Features secure electronic data signatures and comprehensive user auditing logs to prevent record alterations.

2. Built-In Diagnostic Peripherals

  • Integrated Thermal Printer: Prints physical validation receipts directly on-site for immediate cleanroom logbook physical documentation.

  • Multi-Sensor Expansion: Accommodates optional climatic probes to measure ambient temperature, relative humidity, and differential air velocity alongside particulate metrics.

Targeted Cleanroom Industry Applications

The portable, high-flow design of the 3900 Series makes it a primary validation asset across multiple sectors:

  • Pharmaceutical Cleanrooms: Ensuring immediate compliance during sterile processing, drug compounding, and fill-finish cycles.

  • Semiconductor Manufacturing: Isolating killer sub-micron particulate sources on wafer transport lines and lithography bays.

  • Hospital Operating Rooms: Validating critical surgical suites and sterile pharmacy workspaces to maximize patient safety.

  • Medical Device Packaging: Maintaining clean manufacturing spaces for the assembly and sealing of critical surgical implants.

 

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