Austrálie - angličtina - Department of Health (Therapeutic Goods Administration)

koala medical pty ltd - 14155 - trocar, abdominal - a surgical instrument which is supplied sterile and features a sharp pyramidal or conical point used to puncture the abdomen wall. it can be assembled and used together with a compatible sleeve filling its lumen thereby allowing the introduction of this assembly. following puncture, the trocar is withdrawn providing a working channel to the cavity.

Austrálie - angličtina - Department of Health (Therapeutic Goods Administration)

koala medical pty ltd - 14155 - trocar, abdominal - a surgical instrument which is supplied sterile and features a sharp pyramidal or conical point used to puncture the abdominal wall. it can be assembled and used together with a compatible sleeve filling its lumen, thereby allowing the introduction of this assembly. following puncture, the trocar is withdrawn providing a working channel to the cavity. the tropian trocar may have a filter which provides filtration and/or removal of particulates and odours generated during surgical procedures in which there maybe tissue ablation.

Austrálie - angličtina - Department of Health (Therapeutic Goods Administration)

c r kennedy & co pty ltd - 13375 - retractor, abdominal - a surgical instrument intended for separating the edges of an abdominal incision to expose or access organs or tissues to permit examination or intervention.

Austrálie - angličtina - Department of Health (Therapeutic Goods Administration)

kci medical australia pty ltd - 61147 - negative-pressure wound therapy open-abdomen dressing - indicated for temporary bridging of abdominal wall openings where primary closure is not possible and or repeat abdominal entries are necessary. the intended use of this dressing is for use in open abdominal wounds, with exposed viscera, including but not limited to abdominal compartment syndrome. the intended care setting is a closely monitored area within the acute care hospital, such as the icu. the abdominal dressing will most often be applied in the operating theater.

Austrálie - angličtina - Department of Health (Therapeutic Goods Administration)

medtronic australasia pty ltd - 46777 - abdominal aortic aneurysm stent - the stent graft system when placed within the target lesion, provides a permanent, alternative conduit for blood flow within the patient's vasculature by excluding the lesion from blood flow and pressure. the stent graft is preloaded into the delivery system and advanced to the aneurysm using fluoroscopic guidance. upon deployment, the stent graft self-expands to conform to the shape and size of the seal zones above and below the aneurysm. the device is a graft system indicated for the endovascular treatment of infrarenal or juxtarenal aortic or aortoiliac aneurysms (with the parallel graft technique) in patients with the following characteristics - adequate iliac or femoral access vessel morphology that is compatible with vascular access techniques, devices, or accessories; iliac distal fixation length of ?15 mm; iliac diameters with a range of 8 to 25 mm; morphology suitable for aneurysm repair; one of the following: aneurysm diameter >5 cm or aneurysm diameter of 4 to 5 cm, which has also increased in size by 0.5 cm in the last 6 months or aneurysm that is at least 1.5 times the diameter of the normal infrarenal aorta. in addition, for treatment of infrarenal abdominal aortic or aortoiliac aneurysms, the following patient characteristics apply: proximal neck length of ?10 mm or ?4 mm and <10 mm when used in conjunction with the heli-fx endoanchor system, with insignificant calcification, or insignificant thrombus with ?60? infrarenal and ?45? suprarenal angulation and a vessel diameter approximately 10% to 20% smaller than the labeled endurant ii/iis stent graft diameter.

Austrálie - angličtina - Department of Health (Therapeutic Goods Administration)

medtronic australasia pty ltd - 46777 - abdominal aortic aneurysm stent - the stent graft system when placed within the target lesion, provides a permanent, alternative conduit for blood flow within the patient's vasculature by excluding the lesion from blood flow and pressure. the stent graft is preloaded into the delivery system and advanced to the aneurysm using fluoroscopic guidance. upon deployment, the stent graft self-expands to conform to the shape and size of the seal zones above and below the aneurysm. the device is a graft system indicated for the endovascular treatment of infrarenal or juxtarenal aortic or aortoiliac aneurysms (with the parallel graft technique) in patients with the following characteristics - adequate iliac or femoral access vessel morphology that is compatible with vascular access techniques, devices, or accessories; iliac distal fixation length of ?15 mm; iliac diameters with a range of 8 to 25 mm; morphology suitable for aneurysm repair; one of the following: aneurysm diameter >5 cm or aneurysm diameter of 4 to 5 cm, which has also increased in size by 0.5 cm in the last 6 months or aneurysm that is at least 1.5 times the diameter of the normal infrarenal aorta. in addition, for treatment of infrarenal abdominal aortic or aortoiliac aneurysms, the following patient characteristics apply: proximal neck length of ?10 mm or ?4 mm and <10 mm when used in conjunction with the heli-fx endoanchor system, with insignificant calcification, or insignificant thrombus with ?60? infrarenal and ?45? suprarenal angulation and a vessel diameter approximately 10% to 20% smaller than the labeled endurant ii/iis stent graft diameter.

Austrálie - angličtina - Department of Health (Therapeutic Goods Administration)

johnson & johnson medical pty ltd - 44756 - abdominal hernia surgical mesh, composite-polymer - proceed? surgical mesh is comprised of an oxidized regenerated cellulose (orc) fabric and a nonabsorbable polypropylene mesh which is encapsulated by a polydioxanone polymer. the polypropylene mesh side allows for tissue ingrowth while the orc side provides a bioresorbable layer that physically separates the polypropylene mesh from underlying tissue and organ surfaces during wound healing period to minimize tissue attachment to the mesh. the polydioxanone provides a bond to the orc layer. proceed? surgical mesh is indicated for the repair of abdominal wall hernias that require the addition of a reinforcing material to obtain the desired surgical result.

Austrálie - angličtina - Department of Health (Therapeutic Goods Administration)

polyspine corp pty limited - 41030 - orthosis, spinal, lumbosacral, pendulous abdomen support - polyspine is a supportive exoskeleton/ activity brace which provides people with moderate to severe physical disability trunk support, enabling them to participate in a range of activities outside of the wheelchair. the spine is the central product , with a range of accessories that will allow it to be used in a range of settings. the polyspine is an externally lumbar and abdomen support device applied to encompass the lumbosacral spine region of the trunk to support or immobilize deformities, fractures, sprains, or strains of the spine, as well as to provide support for a pendulous abdomen. this is a reusable device.

Tanzanie - angličtina - Tanzania Medicinces & Medical Devices Authority

hasafa health sciences limited, tanzania - neoprene abdominal support -

Austrálie - angličtina - Department of Health (Therapeutic Goods Administration)

w l gore & associates (australia) pty ltd - 46777 - abdominal aortic aneurysm stent - the gore? excluder? conformable aaa endoprosthesis is a single-use, permanently implanted device for the treatment of abdominal aortic aneurysm (aaa), an enlargement of the aorta caused by a weakening of the artery wall. the gore? excluder? conformable aaa endoprosthesis may be used to accommodate specific anatomy of an aneurysm. the gore? excluder? conformable aaa endoprosthesis is intended to exclude the aneurysm from the blood circulation in patients diagnosed with infrarenal abdominal aortic aneurysm (aaa) disease and who have appropriate anatomy as described below: ? adequate iliac / femoral access ? infrarenal aortic neck treatment diameter range of 16?32 mm ? a minimum aortic neck length of 10 mm when proximal aortic neck angulation is less than or equal to 60 degrees ? a minimum aortic neck length of 15 mm when proximal aortic neck angulation is less than or equal to 90 degrees ? iliac artery treatment diameter range of 8?25 mm and iliac distal vessel seal zone length of at least 10 mm