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2026 INFECTION CONTROL GUIDELINES
Instrument reprocessing
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Integrating every stage of the reprocessing workflow
From cleaning & disinfection, inspection, maintenance, and packaging to sterilization, documentation, and storage – every stage is organized to support effective infection control.
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STERILIZATION
SterilizersMELAG steam sterilizers are developed for a wide range of applications in clinics and healthcare facilities, with a focus on reliability, efficiency, and process control. Tìm hiểu thêm → |
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LARGE-SCALE STERILIZATION
Large-capacity steam sterilizersThe 100- and 200-liter steam sterilizers are designed for central sterile supply departments (CSSDs), hospitals, and healthcare facilities with high-volume processing requirements. Tìm hiểu thêm → |
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COMPACT AUTOCLAVES
Vacuclave 105 & Vacuclave 305A compact sterilizer range for facilities seeking to optimize space and processing time. Vacuclave 105 & 305 support instrument sterilization on two trays and feature flexDRY drying. Tìm hiểu thêm → |
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CLEANING & DISINFECTION
MELAthermAutomates instrument cleaning and disinfection to standardize cycles, reduce manual handling, and support consistent infection control. Tìm hiểu thêm → |
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PACKAGING
Pouch sealing equipmentSupports stable and secure seals for sterilization packaging, helping protect sterilized instruments from the risk of recontamination. Tìm hiểu thêm → |
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PACKAGING & STORAGE
MELAstoreTray and container systems that help standardize instrument sets and facilitate cleaning, disinfection, packaging, sterilization, and storage. Tìm hiểu thêm → |
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DOCUMENTATION & TRACEABILITY
Reprocessing documentation managementDocumentation and traceability solutions support cycle monitoring, batch release, and information linkage throughout the entire reprocessing workflow. Tìm hiểu thêm → |
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TESTING
Routine testingTesting products support routine evaluation of sterilizers and packaging equipment in accordance with the facility's quality control program. Tìm hiểu thêm → |
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MAINTENANCE
LubricationSuitable maintenance oils and adapters help maintain the operating condition of instruments with moving parts in accordance with the manufacturer's instructions. Tìm hiểu thêm → |
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CONSUMABLES
Accessories & consumablesA range of accessories supporting cleaning, disinfection, maintenance, packaging, sterilization, and documentation throughout the reprocessing workflow. Tìm hiểu thêm → |
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QUY TRÌNH TÁI XỬ LÝ
Reprocess instruments through a standardized workflowThe complete instrument reprocessing workflow includes cleaning, disinfection, inspection, maintenance, packaging, sterilization, documentation, and release. Standardizing these steps supports infection control, reduces the risk of cross-contamination, and facilitates traceability when needed. |
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From used instruments to instruments ready for use
Each step should be carried out in the correct sequence and in accordance with the characteristics of the instruments, equipment, and the manufacturer's instructions.
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01
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Instrument preparationCollect, perform preliminary cleaning, disassemble when necessary, and promptly transport instruments from the treatment area to the reprocessing area.
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02
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Cleaning & disinfectionAutomated washer-disinfectors help standardize the process and control cycle parameters according to defined programs.
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03
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Inspection, maintenance & lubricationAfter cleaning, disinfection, and drying, instruments should undergo visual and functional inspection before proceeding to the next step.
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04
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Đóng góiBefore sterilization, instruments should be appropriately packaged in pouches, packaging materials, or sterilization containers/trays according to process requirements.
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05
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Tiệt khuẩnSuitable instruments are sterilized using saturated steam according to the defined cycle for each load type and the equipment manufacturer's instructions.
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06
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Documentation & releaseComplete the process through inspection, documentation, and release of the processed batch by an authorized person in accordance with the facility's procedures.
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07
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Storage of sterile instrumentsSterilized instruments should be protected from recontamination during transport and storage.
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Clearly separate dirty, clean, and sterile areas
The reprocessing area should be organized as a one-way flow, minimizing cross-over between contaminated instruments and instruments that have been cleaned, disinfected, or sterilized.
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ZONE 01
Dirty zoneReceipt and initial processing of used instruments.
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ZONE 02
Clean zoneInspection, maintenance, packaging, and sterilization preparation.
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ZONE 03
Sterile zoneSterilization, release, and storage of processed instruments.
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Explore more specialized solutions
From protecting surgical instruments to building a centralized reprocessing system, MELAG focuses on systematic, long-term solutions.
Standardize processes – strengthen infection control
From individual instruments to the entire reprocessing system, a properly organized workflow helps create consistency, efficiency, and control in daily practice.
