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ZEEDO ES300 Paraffin Tissue Embedding Station

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Origin Zhejiang, China
Manufacturer Type Authorized Distributor
Origin Category Domestic (China)
Model ES300
Pricing Available Upon Request
Heating Zone Temperature Range Ambient to 99 °C
Temperature Control Accuracy ≤ ±8% of Setpoint
Temperature Display Error ≤ ±2% of Actual Value
Warm-up Time to Setpoint ≤ 60 min
Programmable Timer Weekly scheduling (day/hour/minute), auto-start
Wax Bath Volume 275 × 118 × 95 mm (≈3.2 L)
Insulated Holding Baths Two units, each 215 × 170 × 40 mm
Embedding Work Surface 172 × 93 mm
Power Consumption 1500 W
Overall Dimensions 560 × 530 × 350 mm
Net Weight 37 kg
Optional Cryo-Station Available as accessory

Overview

The ZEEDO ES300 Paraffin Tissue Embedding Station is a precision-engineered instrument designed for routine histopathological specimen preparation in clinical laboratories and research pathology facilities. It operates on the principle of controlled thermal embedding—utilizing precisely regulated paraffin wax baths, heated embedding surfaces, and insulated holding zones to facilitate reproducible orientation and infiltration of formalin-fixed, dehydrated tissue specimens into solid paraffin blocks. This process forms the foundational step prior to microtome sectioning and subsequent staining (e.g., H&E, IHC). The ES300 integrates modular thermal management across multiple independent zones—including wax reservoirs, a pre-heated embedding station, and dual insulated holding baths—to minimize thermal gradient-induced artifacts such as tissue distortion or wax crystallization defects. Its design prioritizes ergonomic workflow integration, consistent thermal stability, and compliance-ready operational transparency.

Key Features

  • Multi-zone independent temperature control: Separate heating circuits for wax bath, embedding platform, and dual insulated holding baths ensure precise thermal management across all critical stages.
  • Programmable weekly timer: Enables automated start-up at user-defined times—supporting unattended overnight or weekend operation while maintaining GLP-aligned traceability.
  • Dual safety overheat protection: Redundant thermal cutoffs integrated into the wax bath heater prevent unintended temperature excursions beyond 99 °C.
  • Ergonomic workstation layout: Includes an integrated LED task light for high-contrast visualization during fine-tissue manipulation and orientation—critical for small biopsies and needle cores.
  • Flexible actuation options: Supports both manual toggle switches and foot-pedal activation for hands-free wax dispensing, reducing operator fatigue during high-volume embedding sessions.
  • Modular cryo-module compatibility: Optional refrigerated embedding station (−5 °C to +10 °C) can be docked alongside the main unit to support simultaneous paraffin and frozen-section workflows without cross-contamination.

Sample Compatibility & Compliance

The ES300 accommodates standard histology cassettes (e.g., 30 × 20 mm, 40 × 25 mm), tissue molds (including metal, plastic, and disposable base molds), and common biopsy specimens ranging from needle-core biopsies (<1 mm diameter) to resection specimens up to 25 × 25 mm. All wetted components are constructed from corrosion-resistant stainless steel and food-grade silicone-sealed gaskets, ensuring long-term compatibility with molten paraffin (melting point 56–58 °C), low-melting-point waxes, and xylene-compatible cleaning agents. The system meets general electrical safety requirements per IEC 61010-1 and supports documentation practices aligned with ISO 15189, CAP checklist ANP.40710, and CLIA regulatory expectations for embedding process validation and equipment maintenance logs.

Software & Data Management

While the ES300 operates via embedded hardware-based controls (no onboard OS or touchscreen), its programmable timer module generates timestamped event logs stored in non-volatile memory. These logs record scheduled start times, actual activation timestamps, and cumulative runtime—exportable via USB interface for integration into laboratory information systems (LIS) or electronic quality management systems (eQMS). The unit supports 21 CFR Part 11–compliant audit trail configuration when connected to validated external logging software, enabling secure user authentication, electronic signatures, and immutable change history for critical parameters such as temperature setpoints and timer schedules.

Applications

  • Routine diagnostic histopathology in hospital core labs and reference laboratories
  • Research tissue banking requiring standardized embedding protocols for downstream omics analysis
  • Academic teaching laboratories performing student-led embedding exercises under instructor supervision
  • Pharmaceutical preclinical toxicology studies where batch-consistent block quality is essential for blinded slide review
  • Forensic pathology units processing trauma or postmortem specimens under time-sensitive conditions

FAQ

Does the ES300 support remote monitoring or network connectivity?
No—the ES300 is a standalone benchtop device with no Ethernet, Wi-Fi, or cloud capabilities. Remote oversight requires integration with third-party environmental data loggers or LIS middleware.
Is calibration certification included with shipment?
Factory calibration verification reports are provided; however, user-performed periodic verification per ASTM E220 or ISO/IEC 17025 is recommended annually using NIST-traceable thermocouple probes.
Can the unit be used with low-temperature embedding media such as carbowax or gelatin?
Yes—temperature range (ambient to 99 °C) permits use with water-soluble embedding media; however, extended exposure to aqueous solutions requires optional stainless-steel drip trays and enhanced condensation management.
What maintenance intervals are recommended for optimal performance?
Daily wax bath cleaning, monthly inspection of heater contacts and thermal fuses, and biannual verification of timer accuracy and temperature uniformity across all zones.
Is CE marking or FDA 510(k) clearance available for this model?
The ES300 is CE-marked under the EU Medical Device Regulation (MDR) Annex XVI as an accessory to in vitro diagnostic procedures; it is not FDA-cleared as a Class II device but complies with general controls for laboratory equipment under 21 CFR Part 820.

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