
[Insert Schematic Diagram Here: Simplified autoclave cross-section with numbered parts]
The autoclave sterilization chamber is made from SUS 316L stainless steel which ranges from 3mm to 6mm thickness and meets ASTM A240 standards.
The sterilization chamber design options include circular or rectangular models that function at pressures up to 40 psi.
용량: 25L (dental) to 1,500L (hospital CSSD)
Sealing Mechanism:
Silicone gasket (Shore A 50–60 hardness)
Pneumatic or manual locking (3–5 locking bolts)
안전 기능:
Pressure interlock prevents opening above 0 psi
Thermal shield reduces surface temp to <50°C
Component | Specification | 기능 |
---|---|---|
Jacketed Chamber | 10mm insulation layer | Prevents heat loss |
증기 발생기 | 4–15 kW output | Produces 97% dry saturated steam |
Pressure Sensor | 0–50 psi range ±0.1% accuracy | Monitors cycle progress |
Thermostatic Trap | Opens at 100°C ±2°C | Removes condensate |
Vacuum Pump: 60–100 mbar residual pressure
The vacuum system eliminates 99.9% of air within two minutes following EN 13060 standards.
애플리케이션: Textiles, wrapped instruments, porous loads
UI Types:
Basic: LED indicators + mechanical timers
Advanced: 7″ touchscreen with data export
Validation-Ready Features:
USB/Bluetooth cycle data download
Password-protected parameter adjustment
Critical Component Lifespan:
Part | Replacement Interval | Failure Consequences |
---|---|---|
Door Gasket | 800–1,200 cycles | Steam leaks, aborted cycles |
Steam Generator Coil | 5–8 years | Reduced steam quality |
Solenoid Valves | 3–5 years | Pressure regulation failures |
Material Selection Guide:
애플리케이션 | Preferred Material | Rationale |
---|---|---|
Chamber Interior | SUS 316L | Chloride corrosion resistance |
Steam Lines | ASTM A106 Gr.B | High-temperature durability |
Electrical Contacts | Silver-Nickel Alloy | Oxidation prevention |
When purchasing autoclaves distributors need to validate these parameters.
Chamber Certification:
The autoclave chamber needs to have an ASME BPVC Section VIII stamp for pressure vessels certification.
Passivation certificate (ASTM A967)
Steam Quality Metrics:
Dryness fraction: ≥97%
Non-condensable gases: ≤3.5% (EN 285 standard)
Vacuum Performance:
The air removal rate must result in ≤1% residual air to pass the Bowie-Dick test.
에너지 효율성:
The steam usage rate stands at no more than 5 kilograms for every 100 liters of chamber volume.
Preventive Schedule:
Task | Frequency | Tools Required |
---|---|---|
Gasket Inspection | Weekly | Leak detection spray |
Calibration Check | Quarterly | NIST-traceable pressure gauge |
Chamber Descaling | 500 cycles | 10% citric acid solution |
일반적인 문제 해결:
Problem: Incomplete drying 솔루션: Clean strainer in exhaust line
Problem: Error code “E3” (low water) 솔루션: Check float switch alignment
Medical buyers prioritize autoclaves meeting:
ISO 13485: Quality management for medical devices
EN 13060: Small steam sterilizer standard
21 CFR 880.6860: FDA performance criteria
Documentation Checklist:
Material test certificates (MTC) for chamber
Pressure equipment directive (PED) compliance
Electromagnetic compatibility (EMC) test reports
IoT Integration:
Real-time part wear monitoring via strain gauges
Sustainable Materials:
Graphene-coated chambers for enhanced corrosion resistance
Additive Manufacturing:
3D-printed steam nozzles optimized for flow dynamics
Medical equipment distributors who understand autoclave components gain a competitive edge. Buyers achieve global standard sterilization solutions with minimal downtime by thoroughly evaluating chamber materials and steam systems alongside control interfaces. Predictive maintenance strategies in healthcare facilities will drive the market for smart diagnostic modular autoclaves as the dominant force in the $3.2 billion sterilization equipment sector.
Q1: How often should door seals be replaced? A: Every 1,200 cycles or if visible cracks/compression set exceeds 15%.
Q2: Can chamber material impact sterilization efficacy? A: Yes. Pitted surfaces trap contaminants – SUS 316L maintains smoothness for 10,000+ cycles.
Q3: What’s the cost difference between basic and advanced control panels? A: Touchscreen models cost 25–40% more but reduce validation time by 70%.
Q4: How to verify vacuum pump performance? A: Conduct daily air leakage tests – pressure rise ≤1 mbar/min indicates proper function.
Q5: Are stainless steel trays mandatory? A: Aluminum trays are acceptable but require passivation every 6 months (ASTM A967).
Equip your clients with technologically advanced autoclaves built for precision and compliance.
📧 이메일: inquiry@shkeling.com 📱 WhatsApp: +86 182 2182 2482 🌐 Explore Models: Industrial & Portable Autoclaves
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Certified Excellence: CE, ISO 13485, and FDA-compliant designs
Custom Engineering:
Dual-door pass-through configurations
Left/right-handed door options
B2B Benefits:
Bulk pricing for 10+ units
Spare parts inventory access
Multilingual installation guides
Limited-Time Offer: ✅ Free component lifetime calculator with quote request ✅ Priority technical support for distributors
멸균은 의료 시설과 실험실 환경 모두에서 감염 관리 관행의 필수 요소로 작용합니다. 증기를 통한 오토클레이브 멸균은 많은 응용 분야에서 효과적이지만 다음과 같은 경우 최적이 아닌 것으로 입증되었습니다.
전 세계 의료 전문가들은 의료 기기의 안전과 멸균을 보장하기 위한 필수 도구로 오토클레이브를 신뢰합니다. 의료 기기 유통업체와 조달 전문가는 오토클레이브의 원리와 이점을 이해해야 합니다.
의료 기술의 발전으로 의료 기기를 항상 안전하게 멸균 상태로 유지하는 것이 필수적입니다. 의료 기기 유통업체, 딜러, 조달 전문가는 효과적인 운영을 위해 멸균 방법을 이해해야 합니다. 의료 기기의
의료 기기 및 기구 멸균에는 환자의 안전을 보호하고 규제 표준 준수를 용이하게 하기 때문에 오토클레이브가 필요합니다. 가장 정교한 오토클레이브 시스템도 여전히 몇 가지 한계가 있습니다. 의료 기기 유통업체,
의료 기기 제조에서 오토클레이브는 다양한 기기와 재료에 대해 일관된 멸균을 제공하기 때문에 필수적인 장비로 작용합니다. 오토클레이브는 고압 포화 증기를 사용하여 박테리아, 바이러스, 곰팡이, 세균을 박멸합니다.
오토클레이브는 의료 및 과학 환경에서 기기와 재료를 지속적으로 멸균하여 중요한 역할을 하는 장비입니다. 의료 장비 유통업체와 딜러 및 조달 전문가는 오토클레이브의 기능을 유지해야 합니다.