Home Precision Environment Particle Counting & Monitoring Portable Particle Counters 3900 Series
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KanomaxHandheld & Portable Particle Counters

Portable Particle Counters 3900 Series — 3905 / 3910 / 3920

Portable particle counters at 28.3 / 50 / 100 LPM with 6.4-inch colour touchscreen and built-in thermal printer. 21 CFR Part 11 compliance option for pharmaceutical cleanroom certification.

Flow rates
3905: 28.3 LPM (1.0 CFM) / 3910: 50 LPM / 3920: 100 LPM (3.53 CFM)
Channels
6: 0.3–10.0 µm (3905/3910); 0.5–10.0 µm (3920)
Display
6.4-inch colour touchscreen
Compliance
ISO 21501-4; 21 CFR Part 11 option; IQ/OQ documentation
PortableCleanroomParticle counting
ISO 21501-4ISO 14644-1ISO 14644-221 CFR Part 11EU GMP Annex 1

Products

ModelGroupPositioningCore fit
3905Portable OPC — 1.0 CFMPortable 6-channel OPC at 28.3 LPM — ISO Class 2 capableCleanroom certification, filter testing, pharmaceutical
3910Portable OPC — 1.77 CFMPortable 6-channel OPC at 50 LPMFaster cleanroom certification, large-area surveys
3920Portable OPC — 3.5 CFMPortable 6-channel OPC at 100 LPM — higher flow for lower classification limitsISO Class 4–9 large-area, high-speed sampling

Key Features

Three flow rates — 28.3, 50 and 100 LPM

The 3905 (28.3 LPM), 3910 (50 LPM) and 3920 (100 LPM) allow selection matched to ISO 14644-1 minimum sample volume requirements. The 3920 at 100 LPM dramatically reduces per-sample time in ISO Class 5–6 large-volume rooms, shortening certification campaign duration without compromising statistical confidence.

6.4-inch touchscreen + built-in thermal printer

The large colour touchscreen simplifies sample plan programming in cleanroom gowning. The integrated thermal printer produces on-site paper records at each sample point — essential for immediate sign-off and reducing transcription risk. No need to carry a separate printer.

21 CFR Part 11 electronic records option

Optional FDA 21 CFR Part 11 compliance with electronic signature, tamper-evident audit trail and validated data storage. IQ/OQ documentation kit supports GxP system validation requirements for pharmaceutical facility computer system validation (CSV) packages.

Environmental sensor alongside particle counts

The environmental sensor records air velocity, temperature, relative humidity and pressure during particle counting — combining cleanroom classification and airflow verification in one instrument pass, reducing total qualification time.

Ethernet, USB and memory card for data transfer

Ethernet, USB and an MMC memory card slot support transfer to facility monitoring systems — eliminating post-run USB data download delays in multi-room certification campaigns.

Technical Specifications

Model comparison — 3905 / 3910 / 3920

Where the three models differ. All remaining specifications are common to the series.
Parameter390539103920
Flow rate1.0 CFM (28.3 L/min)1.77 CFM (50 L/min)3.5 CFM (100 L/min)
Measuring particle size0.3, 0.5, 1.0, 3.0, 5.0, 10.0 µm0.5, 0.7, 1.0, 3.0, 5.0, 10.0 µm
Counting efficiency50 ± 20% at 0.3 µm50 ± 20% at 0.5 µm
Concentration limit500,000 particles/ft³ at 10% coincidence loss300,000 particles/ft³ at 10% coincidence loss

Common specifications

ParameterUnitValue / Description
OPTICAL SENSOR
Light sourceLaser diode
Zero count levelcountsLess than 1 count / 5 minutes
SAMPLING
Sampling time6 s to 23 h 59 min 59 s (configurable)
Interval time6 s to 23 h 59 min 59 s (configurable)
USER INTERFACE
Display6.4 inch colour touch screen
PrinterBuilt-in thermal printer
Data storagedata points10,000
COMMUNICATION
InterfaceEthernet, USB, memory card slot (MMC)
DATA INTEGRITY
SecurityPassword authentication and management, secure data and audit trails (meets 21 CFR Part 11 compliance)
Report formatsISO 14644-1, GB/T16292-2010, Federal Standard, British Standard, EU GMP
ENVIRONMENTAL SENSOR
Measured parametersAir velocity, temperature, relative humidity and pressure
POWER
SupplyAC 100 – 240 V or Li-ion battery
PHYSICAL
Dimensions W × D × Hinch7.9 × 7.9 × 8.1
Weightkg6.44 (14.2 lbs)
STANDARDS & SUPPORT
StandardsISO 21501-4, JIS B9921, CE
Warrantyyears2
Supplied withQuick-start guide, AC adapter, zero filter, isokinetic probe with 2 m (79 inch) tubing, inlet nozzle

Specifications follow the current manufacturer product data (Kanomax 3900 Series, verified 29 August 2026). Values are summarized for page-level selection. Confirm final model configuration, accessories and calibration certificate before order placement.

Applications

ISO 14644-1 / EU GMP Annex 1 certification

ISO Class 5–7 cleanroom certification and EU GMP Annex 1 Grade A/B/C/D classification with 21 CFR Part 11 compliant electronic data trail for FDA-inspected facilities.

Isolator and RABS qualification

High-flow (100 LPM) sampling for RABS and isolator qualification. 21 CFR Part 11 electronic records for FDA Biologics CMC documentation.

ISO 13485 cleanroom periodic classification

ISO 14644-2 periodic classification monitoring and trending for ISO Class 7–8 medical device cleanrooms under ISO 13485.

Accelerated volume sampling

100 LPM (3920) reduces sample time in ISO Class 5 semiconductor fabs — faster classification turnaround during scheduled maintenance windows.

AHU commissioning and filter acceptance

Post-installation HEPA filter acceptance and cleanroom classification after HVAC commissioning. Combined velocity + particle measurement with optional hot-wire probe.

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