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NovoClean Instruments

NW-3100X Pro

A 100 L/min fixed-flow particle counter for pharmaceutical cleanroom routine monitoring, validation, and high-flow sampling, with user permissions, audit trail functions, data export, and printing configuration.

Key Specification

100 L/min fixed flow

Key Specification

Starts at 0.3 μm

Key Specification

8 particle channels

Key Specification

User permissions and audit trail

Pharmaceutical cleanroomsElectronics manufacturingCleanroom validationThird-party testing
NW-3100X Pro
100 L/min
Starts at 0.3 μm
8 channels

Application Scenarios

  • Pharmaceutical cleanroom routine monitoring
  • Cleanroom validation
  • High-flow sampling
  • Third-party testing and field inspection

Key Specifications and Advantages

100 L/min fixed flow
Designed for high-flow sampling and cleanroom validation, reducing sampling time for the same sample volume.
Starts at 0.3 μm
Compared with models starting at 0.5 μm, it also records changes in the 0.3-0.5 μm range for finer particle-contamination trend analysis, where the URS or validation plan requires a 0.3 μm channel.
8 particle channels
Supports eight channels at 0.3, 0.5, 0.7, 1.0, 2.0, 3.0, 5.0, and 10.0 μm.
Records and data functions
User permissions, audit trail, USB data export, and built-in printing are standard. The Bluetooth dot-matrix printer and barcode scanner are optional; other special requirements can be evaluated for customization.

Instrument Functions and Data Integrity

The standard configuration includes user permissions, audit trail, USB data export, built-in printing, and area, room, sampling-point, task, and record management. The Bluetooth dot-matrix printer and barcode scanner are optional; other special requirements can be evaluated for customization.

Field Operation

Touchscreen operation and mapped sampling locations are standard; the barcode scanner is optional.

Data Records

Data trends, audit trail functions, and user permission management.

Output and Options

USB data export and built-in printing are standard. The Bluetooth dot-matrix printer is optional; other special output requirements can be evaluated for customization.

Regulatory Requirements Review

User permissions, audit trail, and data-tamper controls can be demonstrated. Fit with a specific regulation or customer URS requires item-by-item review of implementation, risk assessment, and validation evidence.

Related Products

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Best suited for

Suitable for pharmaceutical cleanrooms, cleanroom validation, routine inspection, and third-party testing.

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Best suited for

For semiconductor cleanrooms, precision electronics manufacturing, and ultra-clean environments requiring monitoring from 0.1 μm.

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Semiconductor cleanrooms / Precision electronics / Ultra-clean environments

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Best suited for

Suitable for aseptic manufacturing, pharmaceutical cleanrooms, and microbial monitoring in controlled areas.

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