Medical CE

The E>Eye for dry eye syndrome treatment has a Medical CE certification (European Standard). The Medical CE certification is a European standard.

TGA registration

The E>Eye IPL device has been registered at the Australian Therapeutic Goods Administration for the treatment of dry eye syndrome. So it is now also TGA registered in Australia.

ISO 9001 and ISO 13485 certifications

E-Swin, the French manufacturer of the E>Eye IPL device has an ISO 9001 certification for the Quality of their Management System to insure they meet the needs of their customers.

E-Swin also has an ISO 13485 certification for the design and manufacturing of medical devices.

WAND Notification

(for New Zealand)
The E>Eye has been notified in the WAND registry.