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Medical Conical Joint Comprehensive Performance Tester is a professional, top-tier laboratory verification system engineered and manufactured by Peyotal to evaluate the rigorous physical and fluidics performance of 6 percent (Luer) conical connectors. Backed by years of specialized manufacturing experience in medical device testing engineering, this automated tester serves as an all-in-one quality assurance platform for leading medical factories, global laboratory networks, and national scientific regulatory departments.
Standards: Fully compliant with leading international and national calibration frameworks including GB1962.1-2015, GB1962.2-2001, ISO 80369-3:2016, ISO 80369-6:2016, and ISO 80369-7:2021.
| Model | PYT-369 |
| Brand | Peyotal |
| Testing Capability | 7-in-1 Comprehensive validation (Liquid/Air leakage, Separation force, Stress cracking, Anti-loosening, Overload resistance). |
| Standard Compliance | ISO 80369-3 / ISO 80369-6 / ISO 80369-7 / GB1962.1 |
| Equipment Weight | 40 kg heavy-stabilized industrial framework |
| )Warranty | 12 months |
Q1: What distinct ISO 80369 product test items can this comprehensive machine execute?
A: This ultimate platform completely replaces the need for separate machines by packing 7 critical evaluation modes into a single framework. It seamlessly runs pressure decay leakage tests, positive pressure liquid leakage tests, sub-atmospheric air leakage rate tests (when equipped with our negative pressure rate tester module), stress cracking analysis, resistance to axial disengagement (separation force), resistance to rotational disengagement (anti-loosening force), and heavy overload resistance validation.
Q2: What is the exact step-by-step mechanical principle for evaluating a 6% (Luer) conical joint?
A: The workflow relies on simultaneous multi-axis force loading to match international regulations. According to the precise criteria of ISO80369-3:2016, ISO80369-6:2016, and ISO80369-7:2021, the machine secures the joint sample and automatically applies a pre-calculated combination of rotational torque and vertical axial force. The system then drives the integrated fluid pump to introduce water pressure or pull a vacuum, automatically analyzing if any structural micro-cracks occur, measuring the exact force needed for disengagement, and tracking leakage values down to the decimal point.
Q3: How does the Peyotal system guarantee data integrity and audit readiness for global laboratory inspections?
A: For medical syringe manufacturers and national science departments, data security is paramount during quality audits. Our 7-inch touchscreen software is engineered around strict GMP multi-level user permission frameworks. Operators can view and log testing data in real-time, but the historical data repository is non-modifiable, creating an permanent audit trail that records every calibration change and test cycle. Results can be printed instantly via the on-board printer to create identical physical verification sheets for laboratory validation logs.
Q4: Does the instrument package arrive as a fully complete solution, and what are the logistics specifications?
A: Yes, Peyotal provides a complete Turnkey setup designed for smooth installation in facilities throughout Latin America, Africa, Central Asia, and Southeast Asia. The unit runs on standard AC 220V/50Hz power and weighs 40kg, giving it immense structural stability during heavy 200N tensile pulling tests. The delivery container arrives factory-sealed with the main testing instrument, a dedicated set of high-durability Luer connector fixtures, a full connector adapter kit covering sizes 0 to 13, our high-performance fluid pressure pump, power cables, and micro-printer paper rolls included.