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GuanCe Instruments GC-X4015 X-ray Foreign Object Detection System

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Brand GuanCe Instruments
Origin Beijing, China
Manufacturer Type Authorized Distributor
Regional Classification Domestic (China)
Model GC-X4015
Power Supply AC 220 V, 50–60 Hz
Automation Level Fully Automatic
Detection Channel Height 100 mm
Effective Detection Width 400 mm
X-ray Leakage Rate <1 µSv/h (compliant with FDA 21 CFR Subchapter J & EU CE Directive 2013/35/EU)
Minimum Detectable Stainless Steel Sphere Ø0.3 mm
Minimum Detectable Stainless Steel Wire 0.2 mm × 2 mm
Minimum Detectable Ceramic/Glass Sphere Ø1.0 mm

Overview

The GuanCe Instruments GC-X4015 X-ray Foreign Object Detection System is an industrial-grade, fully automated non-destructive testing (NDT) platform engineered for high-reliability contaminant identification in food, pharmaceutical, chemical, and consumer goods manufacturing environments. It operates on the fundamental principle of differential X-ray attenuation: a low-energy X-ray beam (typically 60–90 kVp, adjustable via firmware) penetrates conveyed products; materials with higher atomic number (Z) or density—such as stainless steel, aluminum, glass, ceramic, stone, bone, or dense plastics—attenuate the beam more strongly than organic matrices (e.g., meat, dairy, powders, gels). The resulting transmission profile is captured by a high-resolution line-scan detector array (1024–2048 pixel resolution), digitized, and processed in real time to generate grayscale radiographic images. Unlike optical or electromagnetic metal detectors, the GC-X4015 detects both metallic and non-metallic contaminants without requiring conductive or ferromagnetic properties—making it indispensable for inspecting products in metallized film, aluminum trays, glass jars, or thick-walled plastic containers where conventional methods fail.

Key Features

  • Fully automatic operation with integrated conveyor synchronization and programmable rejection logic—designed for seamless integration into continuous production lines operating at speeds up to 1.2 m/s.
  • 15-inch industrial-grade capacitive touch display with intuitive HMI interface; embedded self-learning algorithm automatically calibrates detection thresholds based on product signature, eliminating manual parameter tuning for routine changeovers.
  • Region-of-interest (ROI) masking capability: users define exclusion zones (e.g., metal end-caps on sausages, foil seals on pouches) to suppress false positives while maintaining full sensitivity across critical inspection areas.
  • Comprehensive hardware and software safety architecture: dual-channel door interlock system, real-time beam status monitoring, and immediate X-ray shutdown (<100 ms response) upon cabinet access violation—fully compliant with IEC 61000-6-4 (EMC) and IEC 62471 (photobiological safety).
  • High-contrast imaging engine optimized for low-Z material differentiation: enables discrimination between mineral-based contaminants (e.g., calcified bone vs. quartzite stone) and polymer-based anomalies (e.g., hardened rubber vs. PET fragment) via multi-threshold gray-level analysis.

Sample Compatibility & Compliance

The GC-X4015 accommodates diverse sample formats without mechanical modification: flexible packaging (PET/Alu laminates), rigid containers (glass jars, tin cans), bulk solids (granules, flakes, frozen blocks), and unpackaged items on belt conveyors. Its 400 mm effective width and 100 mm vertical clearance support standard industry packaging dimensions—including tray-sealed ready meals, vacuum-packed meats, and beverage cartons. All radiation safety protocols meet U.S. FDA 21 CFR Part 1020.40 (X-ray equipment performance standards) and EU Council Directive 2013/35/EU on electromagnetic fields. System validation documentation supports IQ/OQ/PQ execution under GMP (21 CFR Part 211) and HACCP frameworks. Image archives and audit logs comply with ALCOA+ principles for data integrity in regulated environments.

Software & Data Management

The proprietary GuanCe VisionSuite v3.2 firmware includes DICOM-compliant image export, timestamped event logging, and configurable user roles (Operator, Supervisor, Administrator) with password-protected access levels. Detection results are stored with full metadata: product ID, batch number, inspection timestamp, ROI map, and raw projection data. Software supports optional 21 CFR Part 11 compliance modules—including electronic signatures, audit trail with immutable timestamps, and role-based permission controls—for pharmaceutical and medical device applications. Export formats include PNG, TIFF, CSV (detection statistics), and XML (structured inspection reports). Remote diagnostics and firmware updates are supported via secure TLS-encrypted Ethernet connection.

Applications

  • Food processing: detection of stainless steel shavings in ground meat, glass fragments in sauces, calcified bone in poultry products, or stones in dried fruits and nuts.
  • Pharmaceutical manufacturing: verification of tablet/capsule integrity, identification of foreign particulates in lyophilized powders, and inspection of blister-pack seal integrity.
  • Consumer packaged goods: validation of component assembly in electronics housings, detection of tooling debris in injection-molded parts, and quality assurance of sealed hygiene products.
  • Chemical and agrochemical industries: screening of catalyst residues, metal wear particles in lubricants, or clumping agents in granular fertilizers.

FAQ

What types of contaminants can the GC-X4015 reliably detect?
It detects metallic (ferrous, non-ferrous, stainless steel), mineral (glass, ceramic, stone, bone), and high-density polymeric contaminants—including those embedded within dense or multi-layered packaging.
Does the system require radioactive sources?
No. It uses an electrically powered micro-focus X-ray tube (no isotopes); radiation ceases immediately when power is off.
Can the GC-X4015 be integrated with existing production line reject mechanisms?
Yes. It provides standard 24 V DC pulse outputs and Modbus TCP/IP interface for direct communication with pneumatic pushers, diverters, or robotic arms.
Is routine calibration required?
Annual verification using certified reference phantoms (e.g., ISO 15530-3 traceable test objects) is recommended; daily operational checks are automated via built-in self-test routines.
What regulatory documentation is provided with the system?
CE Declaration of Conformity, FDA Radiation Safety Report, IEC 61000-6-3/6-4 EMC test summary, and full technical file per EU MDR Annex II requirements are included in the delivery package.

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