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Hengyi HY-0580 Dual-Arm Electromechanical Fatigue Testing System for Biomaterials

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Brand Hengyi
Origin Shanghai, China
Manufacturer Type Original Equipment Manufacturer (OEM)
Regional Classification Domestic (China)
Model HY-0580 (Dual-Arm) OPG
Price Upon Request
Load Capacity 5000 N
Accuracy Class 0.5
Effective Test Width 380 mm
Effective Stroke 800 mm
Speed Range 1–500 mm/min
Speed Accuracy ±0.5% of reading
Force Resolution ±30,000 counts (full-scale, no range switching)
Dynamic Frequency Range 0.01–200 Hz
Waveform Options Sine, Triangle, Square, Ramp, Trapezoidal, User-Defined
Data Acquisition Rate 10,000 Hz
Displacement & Strain Measurement Accuracy ±0.5% of reading
Power Supply 220 V AC, 50 Hz, 1500 W
Net Weight 180 kg
Dimensions (W×D×H) 680 × 400 × 1420 mm

Overview

The Hengyi HY-0580 Dual-Arm Electromechanical Fatigue Testing System is a precision-engineered platform designed specifically for high-fidelity mechanical characterization of biomaterials, soft polymers, elastomers, and miniature specimens under cyclic loading conditions. Unlike hydraulic or servo-hydraulic systems, this system employs a direct-drive linear motor actuator mounted in an upper-positioned configuration—eliminating the need for hydraulic fluids, lubricants, or complex sealing mechanisms. This architecture ensures clean operation, minimal maintenance, and intrinsic compliance with ISO 17025-accredited laboratory environments where contamination control and long-term calibration stability are critical. The system operates on the principle of controlled displacement-driven fatigue testing, enabling precise imposition of user-defined waveforms—including sine, triangle, square, ramp, trapezoidal, and custom profiles—at frequencies ranging from 0.01 Hz to 200 Hz. Its dual-arm structural frame provides enhanced lateral rigidity and axial alignment stability, essential for reproducible low-force (<5000 N), high-resolution fatigue experiments on delicate biological constructs such as hydrogels, decellularized tissues, electrospun scaffolds, and suture anchors.

Key Features

  • Dual-column rigid frame with T-slot test table for rapid fixture interchangeability and multi-axis alignment flexibility
  • Direct-coupled linear motor actuation—zero backlash, no oil leakage, silent operation, and zero environmental footprint
  • Full-scale force resolution of ±30,000 digital counts without internal range switching; maintains constant resolution across 0.1% to 100% of full scale
  • Real-time data acquisition at up to 10,000 Hz, supporting high-fidelity capture of transient strain bursts, hysteresis loops, and crack initiation signatures
  • Integrated electronic limit protection, overload cutoff (>110% FS), and self-diagnostic routines for drive, sensor, and power subsystems
  • Motorized crosshead with dual-speed (fast/slow) positioning and programmable return-to-origin functionality
  • Compliance with ISO 5893, ASTM E466, ASTM D3479, ISO 1099, and GB/T 2611–2007 and JB 9397–2002 technical specifications

Sample Compatibility & Compliance

The HY-0580 accommodates a broad spectrum of specimen geometries and mechanical behaviors: tensile coupons (ISO 527-2, ASTM D638), compression cylinders (ASTM D695), peel configurations (90°/180° per ASTM D903), shear blocks (ASTM D732), and custom miniaturized implants (e.g., dental pins, orthopedic screws, vascular stent segments). Its 380 mm effective width and 800 mm vertical stroke support both standard and application-specific fixtures—including pneumatic grips, cryo-clamps, fluid immersion chambers, and environmental shrouds (operable within 10–35 °C ambient, ≤80% RH, electromagnetic noise <3 V/m). All firmware and software modules adhere to GLP/GMP documentation requirements, including audit-trail-enabled test method versioning, user access controls, and electronic signature support compliant with FDA 21 CFR Part 11 when deployed with validated software packages.

Software & Data Management

Control and analysis are executed via Hengyi’s proprietary TestMaster™ v4.x software suite, built on a modular architecture compatible with Windows 10/11 (64-bit). The interface supports real-time plotting of load vs. displacement, stress vs. strain, hysteresis energy dissipation, cycle-by-cycle modulus tracking, and fatigue life mapping (S–N curves). Raw time-series data is exported in ASCII (.csv), HDF5, or MATLAB-compatible binary formats. Automated report generation includes customizable templates aligned with ISO/IEC 17025 reporting clauses, with embedded metadata (operator ID, calibration certificate IDs, environmental logs, instrument firmware versions). Optional API integration enables bidirectional communication with LIMS platforms (e.g., LabWare, Thermo SampleManager) and statistical process control (SPC) dashboards.

Applications

  • Fatigue endurance evaluation of biodegradable sutures, tissue-engineered constructs, and hydrogel-based drug delivery matrices
  • Cyclic tensile/compression testing of soft robotics actuators and dielectric elastomer membranes
  • Dynamic mechanical analysis (DMA) of thermoplastic elastomers (TPEs), silicone rubbers, and polyurethane foams
  • Adhesion fatigue of pressure-sensitive adhesives (PSAs) and medical skin-contact films under accelerated aging protocols
  • Validation of ASTM F2129 (electrochemical corrosion-fatigue coupling) for metallic implant alloys under simulated physiological loading
  • High-cycle (>10⁶ cycles) reliability screening of micro-electromechanical systems (MEMS) packaging materials

FAQ

What standards does the HY-0580 comply with for biomaterial testing?
It meets the mechanical performance and metrological traceability requirements of ISO 1099, ASTM E466, GB/T 2611–2007, and JB 9397–2002. Custom test methods may be validated against USP , ISO 13485, or ISO 14801 for dental/orthopedic device applications.
Can the system perform sub-ambient or elevated temperature testing?
Yes—when integrated with third-party environmental chambers (e.g., ESPEC, Weiss), the HY-0580 maintains full closed-loop control and data synchronization across −40 °C to +150 °C ranges.
Is the software qualified for regulated environments (e.g., FDA submission)?
TestMaster™ v4.x supports 21 CFR Part 11 compliance when installed with electronic signature modules, audit trail logging, and IQ/OQ documentation packages—available upon request.
What is the minimum resolvable force increment at 5000 N capacity?
With ±30,000-count A/D resolution and 0.5-class accuracy, the smallest detectable force change is approximately 0.167 N across the full range.
How is calibration traceability maintained?
Each unit ships with a NIST-traceable calibration certificate covering force, displacement, and velocity channels, valid for 12 months under normal use conditions. On-site recalibration services are available globally via Hengyi-certified engineers.

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