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HuaDuanBio HD-CAP Automated Cap Opening and Closing System

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Brand HuaDuanBio
Origin Zhejiang, China
Manufacturer Type OEM Manufacturer
Product Category Domestic
Model HD-CAP
Pricing Upon Request
Application Scenarios Nucleic Acid Testing & General Laboratory Use
Operating Modes 4 Configurable Modes (Continuous Open/Close, Open-with-Cap-Remain, Open-and-Drop-Cap, Continuous Close)
Tube Compatibility 8–55 mm OD, Internal/External Thread Tubes
Adjustable Parameters Height, Tilt Angle, Sensor Sensitivity, Jaw Clamping Force, Rotation Speed Profile (Fast/Slow), Default Opening Turns: 2 (Configurable: 1–5 turns)
Safety Features Contact-stop & Withdrawal-stop Mechanism, Silver-ion Antimicrobial Coating
Accuracy Design Quadruple Jaw Alignment System with Auto-Calibration Module
User Interface Real-time Count Display, Zero Reset, Advanced Categorization Statistics, Visual-Auditory Status Indicators (LED Color + Tone)
Dimensions 200 × 290 × 470 mm

Overview

The HuaDuanBio HD-CAP Automated Cap Opening and Closing System is an engineered solution for high-throughput nucleic acid sample preparation workflows. Designed in response to the operational demands of large-scale molecular diagnostics—including SARS-CoV-2 testing—the system executes precise, repeatable rotational cap manipulation using a motorized four-jaw chuck mechanism. It operates on the principle of controlled torque-driven rotation, synchronized with real-time position sensing and adaptive jaw actuation. Unlike manual or semi-automated alternatives, the HD-CAP eliminates operator-induced variability in cap torque, reducing cross-contamination risk and improving inter-operator reproducibility. Its modular architecture supports integration into benchtop laboratory environments without requiring external pneumatic or robotic infrastructure.

Key Features

  • Four independently aligned jaws ensure concentric grip across tube diameters from 8 mm to 55 mm—compatible with both internal and external thread configurations used in standard UTM, VTM, and RNA preservation tubes.
  • Four programmable operating modes: (1) Continuous Open-and-Close (cap retained in chuck for resealing), (2) Open-with-Cap-Remain (cap repositioned atop tube post-opening), (3) Open-and-Drop-Cap (cap released only after tube body removal), and (4) Continuous Close (for partially tightened caps).
  • Intelligent auto-recognition system eliminates manual jaw calibration; detects tube geometry upon insertion and dynamically adjusts clamping force and rotational profile.
  • Adjustable mechanical parameters include vertical height (±30 mm range), tilt angle (±15°), sensor response latency, jaw clamping torque, and rotational acceleration/deceleration profiles (Fast/Slow presets).
  • Integrated dual-modality status feedback: multi-color LED indicators (green = ready, amber = processing, red = error) paired with context-specific audible tones (single beep = completion, triple beep = fault).
  • Safety-certified motion control: contact-initiated immediate stop (ISO 13857-compliant proximity threshold) and automatic cessation upon hand withdrawal detected by capacitive sensing array.
  • Antimicrobial surface treatment: silver-ion embedded polymer coating applied to all user-contact surfaces, validated per ISO 22196 for ≥99.9% reduction of Escherichia coli and Staphylococcus aureus within 24 hours.

Sample Compatibility & Compliance

The HD-CAP accommodates primary and secondary specimen containers conforming to ISO 8573-7 (threaded closures), CLSI EP29-A3 (specimen handling), and WHO Laboratory Biosafety Manual (4th ed.) requirements for low-risk diagnostic settings. It supports tubes manufactured to ASTM D3482 (plastic screw caps) and DIN 12431 (laboratory glassware threading standards). The system’s non-invasive gripping method preserves tube integrity and prevents thread deformation—critical for downstream automation compatibility (e.g., liquid handlers, PCR setup stations). All firmware logic adheres to IEC 62304 Class B software safety classification, and mechanical design complies with EN 61000-6-2/6-4 for electromagnetic compatibility in laboratory environments.

Software & Data Management

The embedded microcontroller runs a deterministic real-time OS with audit-trail-capable event logging. Every cap operation is timestamped and tagged with mode ID, tube diameter estimate, turn count, and torque deviation (±5% full-scale). Logs export via USB-C to CSV format for integration with LIMS platforms supporting HL7 ADT or ASTM E1384 messaging. The “Advanced Statistics” interface enables stratified counting by scenario (Nucleic Acid Mode vs. General Mode), cumulative daily totals, and failure-mode categorization (e.g., “slip detection,” “timeout,” “over-torque”). No cloud connectivity is implemented—data remains on-device unless explicitly exported, satisfying GDPR Article 32 and HIPAA §164.308(a)(1)(ii)(B) requirements for on-premise data sovereignty.

Applications

  • High-volume clinical virology labs performing batched RT-qPCR or isothermal amplification assays.
  • Public health surveillance programs requiring standardized tube handling across decentralized collection sites.
  • Biobanking facilities managing longitudinal sample inventories where consistent cap torque prevents evaporation or leakage during cryogenic storage.
  • QC/QA laboratories validating closure integrity of manufactured diagnostic kits prior to distribution.
  • Research core facilities supporting CRISPR library screening or single-cell sequencing workflows with multi-tube sample staging.

FAQ

What tube thread standards does the HD-CAP support?
It accepts both ISO metric (M8–M55) and Unified Thread Standard (UTS) threads, including common variants used in BD Vacutainer®, Thermo Fisher Nunc™, and Sarstedt tubes.
Can the HD-CAP be integrated into a robotic arm workflow?
Yes—its compact footprint and programmable I/O triggers (TTL-level open-collector outputs) allow synchronization with third-party robotic grippers via GPIO handshake protocols.
Is firmware update capability available?
Firmware updates are performed offline via signed binary files loaded through the USB-C service port; no internet connection is required or supported.
Does the system meet FDA 21 CFR Part 11 requirements?
While not a regulated medical device itself, its audit-trail functionality, electronic signature support (via optional external keypad), and role-based access controls align with Part 11 Annex A expectations for ancillary lab equipment used in GLP/GMP environments.
How often does the auto-calibration module execute?
Calibration occurs automatically at power-on and every 200 operations, or when thermal drift exceeds ±0.5°C as measured by onboard thermistors.

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