Each factsheet provides in-depth look to a specific feature of our latest sterilization technology with big impact on your business!

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STERRAD 100NX ALLCLEAR 1-DOOR

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Inhalation of H2O2 can cause severe irritation of lungs, throat, and nose, which may result in life-threatening complications.

➜ STERRAD® Sterilization Systems reduce residual load emissions to safe levels, ensuring that users, patients and the environment are protected, without the need of weekly chamber leak tests or quarterly gasket inspection required.

➜ In line with the H2O2 emissions thresholds by the American Conference of Governmental Industrial Hygienists (ACGIH®), STERRAD® Sterilization Systems’ reduce emissions at breathing zone level, up to 67 times lower than those from STERIS V-PRO® sterilizers.

➜ Designed to minimize workflow interruptions before they occur, with integrated quality-control features, they reduce delays in instrument throughput and help to enable compliance with instruments’ Instructions for Use (IFU) and hospital policies.

➜ Automatic reconciliation of sterilization cycle and biological indicator records minimizes the potential for human error and keeps data audit-ready, enhancing compliance.

➜ The configuration of STERRAD® 100NX System can be customized to meet the reprocessing requirements of the hospital. With singe or double door options and a selection between different sterilization cycles, the system can be tailored to the types of procedures performed at your hospital ensuring adherence to the chosen policies.

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Designed with simplicity in mind to reduce the potential for human error
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Factsheet 1:

"The Power of Plasma"

Factsheet 2:

"Defining Chamber Capacity"

Designed with simplicity in mind to reduce the potential for human error
Designed with simplicity in mind to reduce the potential for human error

Factsheet 3:

"Enhancing Efficiency and Compliance "

➜ When comparing similar size’ sterilization systems of different manufacturers for their throughput capacity, the configuration of the chamber dimensions plays a critical role in determining usable volume.

➜ Can a system of higher volume fit the same or less sterilization units than another with lower volume? It could!

➜ Find out the Definition of Chamber Capacity and how STERRAD® Systems create a balance between usable capacity, speed and efficiency!

Factsheet 1:

"The Power of Plasma"

Factsheet 2:

"Defining Chamber Capacity"

Factsheet 3:

"Enhancing Efficiency and

Compliance "

Download All Factsheets Here
Designed with simplicity in mind to reduce the potential for human error

Factsheet 4:

"The Importance of Instrument Validation"

Our newest Factsheet is here!

➜ IInstrument validation in adherence with exacting standards, such as ISO 14937, is vital for sterility assurance

➜ Assuming sterility assurance based on similarities with sterilizers which use the same sterilant, rather than instrument validation, risks inadequate sterilization and may put patients at risk of harm

The SSG is a trusted source of reprocessing information, with every listing having undergone rigo-rous validation, as well as approval by the original MDM, providing the difference between assumed and assured sterility

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Factsheet 4:

"The Importance of Instrument Validation"