Bio/Pharmaceut Eto Ethylene Oxide Gas Sterilizer Sterilizing Equipment for Medical Instruments Sterilization

Theory: Pneumatic
Type: Gas Sterilization Equipments
Certification: CE, ISO13485

Product Description

Basic Specifications
Model NO.FST-SIZE
Electric Tension220~380V
LCD DisplayWith LCD Display
MaterialStainless Steel
AlarmsUltra High Temperature Alarm
RecordingInfo Recording & Printing
Doors TypePneumatic Sliding/Revol Door
Capacity Range1cbm to 100cbm
Product Introduction
Our products include the overall facilities of EO sterilization chamber, preconditioning chamber, degassing chamber, and EO waste gas treatment apparatus.
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All products meet the stringent requirements of ISO9001:2008 and ENISO134585:2003/AC2009.
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Innovative hot air heating system technology with utility model patent certification. Leading the ethylene oxide sterilization industry.
Product Visuals
ETO Sterilizer Chamber
Sterilizing Equipment Details
Sterilization Cycle Process
  • Loading: Goods placed in sterilizer and door locked securely.
  • Temperature Adjusting: Reaching 50ºC (approx. 1-2 hours).
  • Pre-Vacuum: Air removal (6-30 minutes).
  • Leak Test: Checking tightness to ensure zero gas leakage.
  • Pre-humidification: Adjusting to 55%RH humidity (1-1.5 hours).
  • EO Injection: Injecting Ethylene Oxide gas (20-30 minutes).
  • Sterilizing: Maintaining conditions for 4-8 hours.
  • Gas Clearing: Residue removal via vacuum (at least 3 cycles).
  • Unloading: Safety unlock and cart removal.

Efficiency: The sterilization chamber can process two batches of cargo within 24 hours.

Detailed Technical Specifications
Technical Category Specifications
Machine TypeEthylene Oxide sterilizers / Sterilization chambers
Chamber Capacity1 to 100 m3
Chamber TypeRectangular type, 1 to 13 pallets (80x120cm)
Doors TypeDouble doors with pneumatic sliding systems
Chamber MaterialStainless steel grade 304 or 316
Hot Water CirculationDouble jacket with 4 circulation systems
SoftwareSiemens PLC Control (Automatic/Manual)
Safety ComplianceSoftware qualified FDA 21CFR part 11
SensorsPressure, temperature, and humidity sensors
Software & Data Processing
Software Report Interface
Data Processing Details
Process Stages & Logistics
EO Process Stages
Container Loading
Service & Support
Pre-Sales Service
  • Drafting technical agreements and protocols
  • Custom manufacturing of equipment
After-Sales Service
  • Installation and operational training
  • Engineers available for overseas machinery service
  • Maintenance, repair, and parts supply
Frequently Asked Questions
Q1: What is the available capacity for the EO sterilization chambers? A: We offer a wide range of capacities from 1 cubic meter (1cbm) up to 100 cubic meters (100cbm), accommodating 1 to 13 pallets.
Q2: Which international standards do your sterilizers comply with? A: Our products are designed to meet ISO9001:2008 and ENISO134585:2003/AC2009 standards, ensuring high quality and safety for medical use.
Q3: How many batches can be sterilized in a day? A: The E.O. gas sterilizer is highly efficient and is capable of processing two full batches of cargo within a 24-hour period.
Q4: What material is used for the sterilization chamber construction? A: The chambers are constructed using high-grade stainless steel, specifically Grade 304 or 316, for maximum durability and corrosion resistance.
Q5: Do you provide support for international customers? A: Yes, we provide comprehensive after-sales support including installation training and have engineers available to service machinery overseas.
Q6: Is the control software compliant with medical data regulations? A: Yes, our control software is qualified under FDA 21CFR part 11, featuring data storage, graphic recording, and safety password administration.

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