E-Vita Open Neo - Graft, vascular, synthetic

Country: Australia

Language: English

Source: Department of Health (Therapeutic Goods Administration)

Available from:

Cryolife Medical (Australia) Company Pty Ltd

Class:

Class III

Manufactured by:

Jotec GmbH Lotzenacker 23, Hechingen, 72379 Germany

Therapeutic area:

35281 - Graft, vascular, synthetic

Therapeutic indications:

The E-vita OPEN NEO implant consists of a vascular graft part and a stent graft part. The vascular graft part of the E-vita OPEN NEO implant has circular crimps that provide the neces-sary form stability and allow to longitudinal stretching for adaption to the anatomy. At the vascular graft part, there is a perfusion branch which may be used for the extracorporeal perfusion during the intervention. E-vita OPEN NEO is intended for the surgical treatment of dissections or aneurysms in the aortic arch and the descending thoracic aorta with or without involvement of the ascending aorta.

Authorization status:

A

Authorization date:

2021-09-13