AUS sets the standard for ultrasound service and support.
Recognized Excellence — Certified. Awarded. Trusted.
Advanced Ultrasound Systems is proud to maintain ISO 13485:2016 certification — the globally recognized standard for quality management in medical device servicing. This rigorous certification reflects our commitment to safety, regulatory compliance, and consistent service excellence across every system we touch. AUS has also been recognized multiple times for outstanding performance, including being named a Top 100 DOTmed Company and receiving the Best of Tulsa Award in the Medical Equipment Supplier category for both 2023 and 2024. These honors reflect our reputation for technical expertise, integrity, and unmatched customer support in the ultrasound industry.

An NQA Accredited Company
ISO 13485 is the quality management system standard for medical device manufacturers and their sub-tier suppliers and subcontractors. Based on the ISO 9001 standard, ISO 13485 includes additional requirements for medical device manufacturers to demonstrate their intent to comply with applicable regulatory and statutory requirements. ISO 13485 is recognized as an aid in supporting compliance with the Medical Device Directive.

DOTmed
Advanced Ultrasound Systems (AUS) has been named top 100 DOTmed Company
ISO 13485 is the quality management system standard for medical device manufacturers and their sub-tier suppliers and subcontractors. Based on the ISO 9001 standard, ISO 13485 includes additional requirements for medical device manufacturers to demonstrate their intent to comply with applicable regulatory and statutory requirements. ISO 13485 is recognized as an aid in supporting compliance with the Medical Device Directive.

ISO 13485 is the quality management system standard for medical device manufacturers and their sub-tier suppliers and subcontractors. Based on the ISO 9001 standard, ISO 13485 includes additional requirements for medical device manufacturers to demonstrate their intent to comply with applicable regulatory and statutory requirements. ISO 13485 is recognized as an aid in supporting compliance with the Medical Device Directive.

ISO 13485 is the quality management system standard for medical device manufacturers and their sub-tier suppliers and subcontractors. Based on the ISO 9001 standard, ISO 13485 includes additional requirements for medical device manufacturers to demonstrate their intent to comply with applicable regulatory and statutory requirements. ISO 13485 is recognized as an aid in supporting compliance with the Medical Device Directive.

