ESCRS congress september 2016
During this congress in September we promoted the SurgiCube as well as the Operio Mobile and other tools.
During this congress in September we promoted the SurgiCube as well as the Operio Mobile and other tools.
Toul Meditech AB is proud to announce that Operio has been cleared by the FDA according to 510(k) and the device can now be marketed in the US. Operio is a portable device for use in a surgical operating room that produces a directed, non-turbulent flow of air to the surgical site during ophthalmic surgery and to the sterile instruments used during surgery.
„At NIIOS we are eager to see how the concept of the SurgiCube concept is disseminated worldwide and we wish SurgiCube International lots of succes!“ Read the complete newsletter via:
After some serious assessments we are happy to announce that SurgiCube is CE marked. The CE marking demonstrates that our device conforms to the Medical Device Directive 93/42/EEC including the “essential requirements” of safety and performance set out in the EU. After registration with the Competent Authority we may place the CE mark upon our products and thereby claim to meet the requirements set out in the directive.
For more information about the CE Mark click on:
CE Mark Medical:
