What should I do if my ASP Laboratory Equipment is 'Unable to Evacuate Chamber'?
To address the issue of being unable to evacuate the chamber in your ASP Laboratory Equipment, ensure the load is dry before starting the cycle. Remove the load and run diagnostics. Reboot the system. If the problem continues, further assistance is needed.
What to do if my ASP Sterrad 100NX says 'Cassette Used, Disposing'?
If the inserted cassette in your ASP Laboratory Equipment does not have any unused cells remaining, it means the cassette is used and needs to be disposed of. You should insert a new cassette.
What to do if the cycle is canceled by operator on ASP Sterrad 100NX Laboratory Equipment?
If the ASP Laboratory Equipment cycle was canceled by an operator, repackage the load and restart the cycle after the cancellation is complete.
How to fix 'H O Curve Area Too Low' error on ASP Sterrad 100NX Laboratory Equipment?
If your ASP Laboratory Equipment displays the message 'H O Curve Area Too Low' it means that the load is absorbing too much peroxide. Remove any absorbing materials from the load, repackage it, and restart the cycle. If the problem continues, further assistance is needed.
What causes 'H O Peak Too Low' on ASP Sterrad 100NX Laboratory Equipment?
If your ASP Laboratory Equipment displays 'H O Peak Too Low', it indicates that the load is absorbing too much peroxide. Remove any absorbent materials from the load, repackage it, and restart the cycle. If the problem persists, further assistance is needed.
What to do for 'Stage Timeout' on ASP Laboratory Equipment?
Remove the load and run diagnostics on your ASP Laboratory Equipment.
What causes 'Pressure Out Of Range (Low)' on ASP Laboratory Equipment?
If your ASP Laboratory Equipment displays 'Pressure Out Of Range (Low)', it indicates a vacuum system malfunction. Remove the load and run diagnostics.
Would you like to troubleshoot my ASP Laboratory Equipment?
To troubleshoot your ASP Laboratory Equipment, remove the load and run diagnostics. If the problem persists, further assistance is needed.
What to do if the ASP Sterrad 100NX 'Cannot Dispose Cassette, Run Diagnostics'?
If the ASP Laboratory Equipment shows that the cassette did not drop into the disposal box, remove the load and run diagnostics.
How do I fix the 'UV Path Is Blocked' error on my ASP Sterrad 100NX?
If your ASP Laboratory Equipment displays 'UV Path Is Blocked', it means that an object is blocking the UV path. Check that the shelves or the load are not obstructing the path. If the problem continues, further assistance is needed.
Instructions on how to navigate and use the user guide for optimal understanding.
Specifies the purpose and application of the STERRAD® 100NX® Sterilization System.
Details the multiphase sterilization process using hydrogen peroxide vapor and plasma.
Guidelines for operator safety, including handling hazardous chemicals and first aid procedures.
Recommendations for protective gear to ensure operator safety during use.
Precautions for safe loading and handling of devices to prevent damage or injury.
Explains the meaning of symbols and text elements used to convey important information.
Specifies the maximum allowable weight for loads based on the selected sterilization cycle.
Lists materials and devices that are commonly sterilized and their compatibility.
Lists items and materials that should not be processed in the sterilizer.
Outlines essential steps for preparing items, including cleaning, rinsing, and drying.
Provides instructions on proper packaging and arrangement of items for effective sterilization.
Initial steps and prerequisites before operating the sterilizer.
Procedures for powering on the sterilizer and initiating the warm-up sequence.
Information on the use and placement of biological indicators for cycle efficacy verification.
Steps for logging into the sterilizer system using operator credentials.
Instructions for correctly placing items onto the sterilizer shelves.
Guide to choosing and initiating a sterilization cycle.
Procedure for safely aborting an ongoing sterilization cycle.
How to initiate diagnostic tests to identify and resolve system issues.
Reference for interpreting system messages and their corresponding actions.
Information on when and how to contact technical support for unresolved issues.
Overview of the different sterilization cycle options available on the system.
Description of the physical components and operational features of the sterilizer.
Information about the hydrogen peroxide cassette and its role in the sterilization process.
List of user-performed maintenance tasks for the sterilizer.
Procedures for safely disposing of used hydrogen peroxide cassettes.
Instructions for loading new paper rolls into the printer.
Guidelines for cleaning the external surfaces of the sterilizer.
Steps to restart or reboot the sterilizer system.
Overview of different types of reports and files accessible on the sterilizer.
Accessing and reviewing records of past sterilization cycles.
Details on the types of reports generated after each sterilization cycle.
Description of the brief report format for cycle completion.
Description of the parametric report format, detailing cycle parameters.
Description of the comprehensive long-format report for detailed analysis.
Introduction to user access levels and supervisor privileges for system management.
Explanation of the different user access levels and their associated permissions.
Navigation to advanced system configuration and management functions.
Settings for alarm volume, language, and various system features.
Managing user accounts, including adding, modifying, and deleting users.
Running system diagnostic tests to identify and resolve issues.
Accessing and managing calibration and diagnostic files.
Configuration of optional features and cycles.
Electrical power requirements for system operation.
Physical dimensions of the sterilizer unit.
Required space around the sterilizer for operation and maintenance.
Operating and storage temperature ranges for the sterilizer.
Duration of each available sterilization cycle.
List of consumables, product codes, and descriptions.
List of additional parts and their corresponding part numbers.
Instructions on how to navigate and use the user guide for optimal understanding.
Specifies the purpose and application of the STERRAD® 100NX® Sterilization System.
Details the multiphase sterilization process using hydrogen peroxide vapor and plasma.
Guidelines for operator safety, including handling hazardous chemicals and first aid procedures.
Recommendations for protective gear to ensure operator safety during use.
Precautions for safe loading and handling of devices to prevent damage or injury.
Explains the meaning of symbols and text elements used to convey important information.
Specifies the maximum allowable weight for loads based on the selected sterilization cycle.
Lists materials and devices that are commonly sterilized and their compatibility.
Lists items and materials that should not be processed in the sterilizer.
Outlines essential steps for preparing items, including cleaning, rinsing, and drying.
Provides instructions on proper packaging and arrangement of items for effective sterilization.
Initial steps and prerequisites before operating the sterilizer.
Procedures for powering on the sterilizer and initiating the warm-up sequence.
Information on the use and placement of biological indicators for cycle efficacy verification.
Steps for logging into the sterilizer system using operator credentials.
Instructions for correctly placing items onto the sterilizer shelves.
Guide to choosing and initiating a sterilization cycle.
Procedure for safely aborting an ongoing sterilization cycle.
How to initiate diagnostic tests to identify and resolve system issues.
Reference for interpreting system messages and their corresponding actions.
Information on when and how to contact technical support for unresolved issues.
Overview of the different sterilization cycle options available on the system.
Description of the physical components and operational features of the sterilizer.
Information about the hydrogen peroxide cassette and its role in the sterilization process.
List of user-performed maintenance tasks for the sterilizer.
Procedures for safely disposing of used hydrogen peroxide cassettes.
Instructions for loading new paper rolls into the printer.
Guidelines for cleaning the external surfaces of the sterilizer.
Steps to restart or reboot the sterilizer system.
Overview of different types of reports and files accessible on the sterilizer.
Accessing and reviewing records of past sterilization cycles.
Details on the types of reports generated after each sterilization cycle.
Description of the brief report format for cycle completion.
Description of the parametric report format, detailing cycle parameters.
Description of the comprehensive long-format report for detailed analysis.
Introduction to user access levels and supervisor privileges for system management.
Explanation of the different user access levels and their associated permissions.
Navigation to advanced system configuration and management functions.
Settings for alarm volume, language, and various system features.
Managing user accounts, including adding, modifying, and deleting users.
Running system diagnostic tests to identify and resolve issues.
Accessing and managing calibration and diagnostic files.
Configuration of optional features and cycles.
Electrical power requirements for system operation.
Physical dimensions of the sterilizer unit.
Required space around the sterilizer for operation and maintenance.
Operating and storage temperature ranges for the sterilizer.
Duration of each available sterilization cycle.
List of consumables, product codes, and descriptions.
List of additional parts and their corresponding part numbers.
General| Cycle Time (Standard) | 47 minutes |
|---|---|
| Weight | 295 kg (650 lbs) |
| Sterilant | Hydrogen Peroxide (59%) |
| Type | Low Temperature Sterilization System |
| Technology | Hydrogen Peroxide Plasma |
| Electrical Requirements | 100-240 VAC, 50/60 Hz |
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