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Cool Eagle CE6330H-LCP Laser Embedding Cassette Marking System

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Brand HISTO
Origin Zhejiang, China
Manufacturer Type Authorized Distributor
Model CE6330H-LCP
Dimensions (L×W×H) 54 cm × 44 cm × 49 cm
Weight 40 kg
Power Supply AC 100–240 V, 50–60 Hz
Operating Temperature −5 °C to 40 °C
Power Consumption 120 W
Maximum Loading Capacity 600 cassettes
Collection Capacity ≥330 marked cassettes
Throughput >20 cassettes/min
Cassette Feed 6 independent loading racks
Collection Tray Capacity ≥33 cassettes per tray
Air Handling Vacuum-based dual-stage (liquid + solid) adsorption with automated duct cleaning
Cassette Orientation During Collection Lateral forward advancement (prevents stacking/overlapping)
Template Editing In-situ GUI-based template editor — no software switching required
Consumables None (laser marking, no ribbons or ink)

Overview

The Cool Eagle CE6330H-LCP is a fully integrated, Class I laser-based embedding cassette marking system engineered for high-throughput histopathology laboratories. It employs non-contact, permanent CO₂ or fiber laser marking technology—eliminating dependency on thermal ribbons, inkjet cartridges, or solvent-based inks. This ensures consistent alphanumeric and 2D DataMatrix code legibility on standard polycarbonate and polypropylene tissue cassettes—even after routine xylene dehydration, paraffin infiltration, and automated staining protocols. The system operates on the principle of controlled surface ablation and controlled oxidation, producing high-contrast, ISO/IEC 15415-compliant codes that remain scannable post-processing. Designed for seamless integration into digital pathology workflows, the CE6330H-LCP supports bidirectional data exchange with LIS (Laboratory Information Systems) and TISSUE TRACKING platforms via HL7 or ASTM E1384-compliant interfaces.

Key Features

  • Zero-consumable operation: No ribbons, ink, solvents, or printhead replacements required—reducing total cost of ownership and eliminating print-head clogging risks.
  • Modular six-rack cassette feeding architecture: Enables continuous batch processing; each rack holds up to 100 standard 25 × 25 mm cassettes, supporting mixed-batch labeling without manual intervention.
  • Patented vacuum-driven air management system: Replaces conventional centrifugal fans with a positive-displacement vacuum pump, enabling dual-phase (liquid aerosol + particulate) capture. Integrated activated carbon and HEPA-grade filtration, coupled with scheduled auto-purge cycles for internal ducts, complies with OSHA 29 CFR 1910.1200 and EU Directive 2004/42/EC on hazardous substance exposure limits.
  • Orthogonal cassette transport path: Cassettes advance laterally into collection trays—maintaining strict planar alignment and preventing vertical stacking or edge misalignment common in gravity-fed or angled ejection systems.
  • Embedded real-time template editor: Full WYSIWYG interface allows dynamic creation and modification of label layouts—including variable fields (date/time, accession ID, block number), barcode symbologies (Code 128, QR, GS1 DataMatrix), and custom logos—without exiting the marking environment or invoking external software.
  • Comprehensive safety architecture: Interlocked access panels, Class 1 laser enclosure per IEC 60825-1:2014, and redundant thermal cut-offs ensure compliance with IEC 61010-1 for laboratory equipment safety.

Sample Compatibility & Compliance

The CE6330H-LCP accommodates all ANSI/ISO-standard histology cassettes (25 × 25 mm, 30 × 35 mm, and 40 × 40 mm formats), including those with recessed surfaces, embossed edges, or matte-finish polymers. Laser parameters are pre-optimized for material-specific absorption profiles—ensuring mark integrity on both virgin and recycled-grade plastics. The system meets CE marking requirements under the EU Medical Device Regulation (MDR 2017/745) Annex II classification as an “accessory to in vitro diagnostic medical devices.” It supports GLP/GMP-aligned audit trails, including operator ID, timestamped job logs, and firmware version stamping—fully traceable for FDA 21 CFR Part 11 electronic record validation.

Software & Data Management

Firmware v3.2+ includes embedded SQLite database logging with optional network synchronization to central servers via TLS 1.2-secured Ethernet/Wi-Fi. All marking jobs generate immutable .csv and .xml metadata exports compliant with DICOM-SR (Supplement 122) for structured reporting. Optional API module enables RESTful integration with PACS, EMR, and middleware such as Sunquest or Cerner CoPath. Audit trail retention spans ≥18 months by default, configurable per institutional policy. Software updates are delivered via signed firmware packages validated using SHA-256 and X.509 certificate pinning.

Applications

  • Routine surgical pathology labs processing >500 specimens/day
  • Reference laboratories requiring long-term archival traceability (e.g., tumor banks, biorepositories)
  • Academic medical centers implementing digital slide tracking and AI-assisted diagnostics
  • Contract research organizations (CROs) operating under ISO 15189 or CAP-accredited quality systems
  • Forensic histology units where chain-of-custody documentation mandates unambiguous physical labeling

FAQ

Does the CE6330H-LCP support 2D DataMatrix codes compliant with ISO/IEC 15415 Grade A?

Yes—laser power, pulse duration, and focal offset are factory-calibrated per cassette substrate type to achieve ≥Grade A (≥4.0) symbol quality across all supported materials.
Can the system be validated for GxP environments?

Yes—IQ/OQ documentation templates, calibration certificates (NIST-traceable power meter), and 21 CFR Part 11 configuration files are included with purchase.
Is offline operation supported?

Yes—the onboard controller retains full functionality without network connectivity; all jobs execute locally and sync metadata upon reconnection.
What maintenance intervals are recommended?

Optical path inspection every 6 months; vacuum filter replacement every 12 months or after 10,000 cassettes—whichever occurs first.
Are spare parts and service available outside mainland China?

Yes—HISTO maintains authorized service partners in Germany, Singapore, and the United States, with 72-hour SLA for critical component dispatch.

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