Leading provider of medical aesthetic solutions in Australia
Devices
100% Australian designed and supported medical aesthetic devices with certification of the latest standards of ISO 13485:2016
Consummable Supplies
Get quality supplies and safety items at competitive prices to support a successful business.
Technical Support
Smooth-running aesthetic systems are key to your success. The Aesthetic Bureau team provides expert support.
"Delivering Results Through Trusted Quality, Knowledge And Innovation"
- Professional
- Australia's #1 Device Repairer
- Trustworthy
Featured Devices
Medical aesthetic devices and equipment
Consumables Supplier For Medical Aesthetic Businesses
Laser/IPL Safety
Aesthetic Bureau offers a wide range of quality laser safety eyewear to provide varying degrees of protection and visible light transmission levels, in a wide selection of frame styles that offer comfort and durability.
The human eye when unprotected is extremely sensitive to laser radiation, and can suffer permanent damage from direct or reflected beams.
Support Equipment
- Our Testimonials
“Xen LED from Aesthetic Bureau is a top-of-the-line facial rejuvenation system that delivers excellent results. The versatile modality complements my treatment portfolio and has been highly beneficial to my practice for advanced tissue healing, reduced recovery times, and improved treatment outcomes and patient satisfaction. Both my patients and therapists have enjoyed fantastic results from using the Xen LED.”​
Dr Michael Zacharia
Dr Mary Dingley
Accredited Quality Management System for Manufacture of Medical Devices
Australian Aesthetic Devices Pty Ltd trading as Aesthetic Bureau are proud to announce that we have certification of the latest standards of ISO 13485:2016 through accreditation with British Standards Institution (BSI).
This indicates we have met all requirements for a comprehensive Quality Management System for the design and manufacture of medical devices for regulatory purposes.
As part of our accreditation, we are required to undergo stringent auditing every 12 months to ensure we continue to meet the highest quality standards recognised worldwide for medical device manufacturing.
Our Medical Aesthetic Devices are Included in the ARTG
In addition, we have achieved CE Marking (under Medical Devices Directive 93/42/EEC) for the manufacture of multi-modality skin surface treatment systems and photobiomodulation systems (i.e. our IPL and LED therapy systems).
All medical device manufacturers marketing their systems in the EU must achieve compliance with the required conformity assessments of this medical directive.
This process includes performance of a risk/benefit analysis regarding the devices, reducing risks to the minimum, adopting adequate safety measures, and fully informing users of any remaining risk.
We use this CE Marking for our Therapeutic Goods Administration (TGA) conformity assessment for inclusion of our medical devices in the Australian Therapeutic Goods Administration (ARTG).
While CE Marking is a European process, regulations in Australia are aligned very closely with Europe. The TGA recognises CE certification for compliance of medical devices with TGA regulatory requirements.
