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How We Can Help

We can provide compliance/validation reports that meet the requirement of AS 5369:2023 to ensure your autoclave meets the dental/medical infection control requirements.

With our calibrated test equipment we can provide accurate and traceable test cycle verification results, as required by independent accreditation groups.

We can advise on the age and condition of your autoclave and recommendation on the expected life, so you can plan a replacement program before the autoclave becomes non- serviceable.

Autoclave Solutions Provided TOP

  • Annual Performance Qualification for accreditation
  • Performance Re-Qualification
  • Preventative Maintenance
  • Installation Qualification
  • Calibration for compliance to Australian Standards AS 5369:2023
  • Comprehensive Breakdown service and repairs
  • Condition and Risk assessment reports

 

Autoclave Performance Qualification (APQ) TOP

As outlined in the Australian Standards the following tests are performed during annual APQ;

  • Cold Spot measurement or confirmation
  • Temperature versus time during a complete sterilisation cycle, at 3 temperature points, using test loads.
  • Calibration Temperature/Pressure/Vacuum
  • Confirmation of cold spot temperature
  • Internal Water and Pressure leakage test
  • Water and Air filters inspection/replacement as needed
  • Door seal and valve seal inspection/replacement as needed
  • Rapid 3 cycle biological testing
  • Dry cycle temperature testing
  • Electrical safety testing and compliance tagging
  • Device specific validation/calibration reports.

 

Autoclave Preventative Maintenance (APM) TOP

A preventative maintenance schedule can be established based on manufacturers recommendations, and the ongoing service requirement. Typically filters should be checked every 6 months during APM and APQ. Performance testing on each occasion and after repairs is also a requirement of the Australian Standards.

Meet Technical Training Requirements TOP

U-Tech Medical understands that specialised training is required to service and calibrate autoclaves. That’s why our technicians undergo full factory training and receive continued refresher training as part of their professional development.  A factory trained technician has specialists’ tools, test equipment, and access to genuine factory certified parts.

We embrace the concept of quality through continual improvement. We understand that regular technical training is required for continued customer satisfaction, and this is the ultimate goal of our QMS process.

What happens in the event of APQ, APM Failure? TOP

The process will stop when a failure or error message occurs and the corrective action will be discussed with the on-site manager or operator. No additional work will be carried out without customer approval.

 

Autoclave Equipment Repairs TOP

We can organise the repair of most recognised autoclaves including but not limited to the following brands:

A qualified service technician can be sent to your site to evaluate the fault and provide a cost assessment for repairs. On most occasions the repair can be performed on-site, however if an unexpected delay occurs, we can usually organise a loan autoclave.

For all your autoclave needs complete the adjacent enquiry form or o or simply ask one our customer service team members on 1300 488 324.

U-Tech Medical is ISO 9001:2015 certified, iPRO Smartek and JAS-ANZ certified.

ISO 9001 2015 is the world’s most widely recognised Quality Management System. This means you are employing the world’s best practice methods, policies and procedures, it helps dental practitioners to meet the expectations and needs of their patients

Q&A’s Autoclave Compliance and Repair Solutions

Yes. The warranty of equipment is not related to the APQ and APM. Validation is also a requirement after completion of repairs or after any re-calibration.

APQ Validation shall be repeated annually and every time significant changes are made. Changes in packaging or loading specification, which would provide a greater challenge to the sterilisation process.

APM every 6 months. Typically during annually APQ, and 6 months after last APQ.

This is not required, however, if you prefer to keep a copy, it is available online SAI Global and type “AS481 5” or AS 4187

As a guide, the Australian Standard, AS4815, and AS4187 are used by operators, manufacturers, and service providers, as the industry standard for autoclaves used in office based medical and dental facilities.

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