Sydney IVF Spermient (K-SISP) - In vitro fertilization culture medium kit Australia - Inggris - Department of Health (Therapeutic Goods Administration)

sydney ivf spermient (k-sisp) - in vitro fertilization culture medium kit

william a cook australia pty ltd - 42850 - in vitro fertilization culture medium kit - sydney ivf spermient is used to separate sperm by density, using density gradient solutions and centrifugation. it removes dead sperm, blood and somatic cells from healthy motile sperm. it is a 100% stock solution which can be diluted with sydney ivf sperm buffer to the required density. sydney ivf spermient is used to separate sperm based on density, using density gradient solutions.

Test Tube Heater Australia - Inggris - Department of Health (Therapeutic Goods Administration)

test tube heater

william a cook australia pty ltd - 46944 - test tube heater - the test tube heater is intended to hold test tubes containing aspirated follicular fluid at a specified temperature.

Torque manipulating device Australia - Inggris - Department of Health (Therapeutic Goods Administration)

torque manipulating device

william a cook australia pty ltd - 46455 - torque manipulating device - intended to aid in the manipulation and control of guide wires.

Vena Cava Filter Extraction/Repositioning Kit - Catheter, snare Australia - Inggris - Department of Health (Therapeutic Goods Administration)

vena cava filter extraction/repositioning kit - catheter, snare

william a cook australia pty ltd - 45162 - vena cava filter extraction/repositioning kit - the device is used to retrieve a vena cava filter using a jugular approach by standard percutaneous entry (seldinger) technique under fluoroscopic control. the system consists of a radiopaque retrieval loop system with a braided platinum wire loop, a radiopaque co-axial retrieval sheath system, an entry needle, a wire guide and a dilator. a radiopaque band on the outer sheath identifies the precise location of the distal tip of the sheath for positioning accuracy. intended for the retrieval of implanted gunther tulip and cook celect vena cava filters using the jugular approach.

Zenith Branch Endovascular Graft - Iliac Bifurcation - Graft, vascular, synthetic Australia - Inggris - Department of Health (Therapeutic Goods Administration)

zenith branch endovascular graft - iliac bifurcation - graft, vascular, synthetic

william a cook australia pty ltd - 35281 - graft, vascular, synthetic - a one-piece graft which has three connected lumens to connect to the common iliac sidebranch and external iliac segments. the graft is manufactured from polyester, and in the common iliac and external iliac sections, is sewn to stainless steel self-expanding z stents. the internal iliac side branch has two reinforcing rings and a contracting nitinol stent. the graft is presented pre-loaded onto a delivery system for percutaneous delivery. the zenith branch endovascular graft ? iliac bifurcation is intended for the endovascular treatment of patients with aorto-iliac or iliac aneurysm, an insufficient distal sealing site within the common iliac artery and having morphology suitable for endovascular repair.

Zenith Dissection Endovascular Stent with the Z-Trak Plus Introduction System - Aortic stent Australia - Inggris - Department of Health (Therapeutic Goods Administration)

zenith dissection endovascular stent with the z-trak plus introduction system - aortic stent

william a cook australia pty ltd - 47685 - aortic stent - the zenith dissection endovascular stent is a one-piece cylindrical device constructed from self-expanding nitinol stent segments sewn together with polyester suture. the stents are uncovered to avoid blockage of dominant spinal cord intercostal arteries and allow for deployment of the stents across branch vessel origins as needed to treat the dissection. the zenith dissection endovascular stent with the z-trak plus introduction system is indicated for the endovascular treatment of patients with symptomatic aortic dissection distal to the left subclavian artery (can be used to provide support to delaminated segments of the aorta typical in dissection) having morphology suitable for endovascular repair, including: a) adequate iliac/femoral access compatible with the required introduction systems; when used together with the zenith tx2 dissection endovascular graft with pro-form. b) radius of curvature greater than 35mm along the entire length of aorta intended to be treated, by the zenith dissection endovascular stent. c) localised angulation less than 45 degrees and d) diameter at intended implant site (measured outer wall to outer wall) of no greater than 38mm (true lumen) and no less than 20mm (total aortic diameter).

Zenith Fenestrated AAA Endovascular Graft - Graft, vascular, synthetic Australia - Inggris - Department of Health (Therapeutic Goods Administration)

zenith fenestrated aaa endovascular graft - graft, vascular, synthetic

william a cook australia pty ltd - 35281 - graft, vascular, synthetic - this modular system self-expands stainless steel stents with braided polyester and monofilament polypropylene suture. each individual device has its own separate delivery system. the bare suprarenal stent of the proximal body graft contains barbs for additional fixation. the scallops and fenestrations is to allow the proximal margin to sit higher and allow uninterrupted blood flow to branch vessels of the aorta. radiopaque markers on the graft are to facilitate fluoroscopic visualisation. the zenith fenestrated aaa endovascular graft is indicated for the treatment of infrarenal abdominal aortic aneurysms (aaas) in high-risk patients who are not suitable for conventional open surgical repair or who are not suitable for repair with a standard zenith endovascular graft, when the aneurysmal disease extends up to the level of the renal arteries.

Zenith TX2 Dissection Endovascular Graft with Pro-Form and the Z-Trak Plus Introduction System - Graft, vascular, synthetic Australia - Inggris - Department of Health (Therapeutic Goods Administration)

zenith tx2 dissection endovascular graft with pro-form and the z-trak plus introduction system - graft, vascular, synthetic

william a cook australia pty ltd - 35281 - graft, vascular, synthetic - the zenith tx2 dissection endovascular graft is constructed of full-thickness, woven polyester fabric sutured with braided polyester and monofilament polypropylene suture to self-expanding stainless steel cook-z stents. the stent graft is fully stented to provide stability and the expansile force necessary to open the lumen of the graft during deployment. the introduction system enables precise placement with the ability to readjust the graft befopre full deployment. the zenith tx2 dissection endovascular stent graft with pro-form and the z-trak plus introduction system is indicated for the endovascular treatment of patients with symptomatic dissection of the descending thoracic aorta having vascular morphology suitable for endovascular repair, including: a)adequate iliac/femoral access compatible with the required introduction systems, b)radius of curvature greater than 35mm along the length of aorta intended to be treated by straight or tapered component c)non-dissected/aneurysmal aortic segments (fixation sites)proximal to the entry tear with a length of at least 20mm, a diameter measured outer wall to outer wall of no greater than 38mm and no less than 20mm, and with localised angulation less than 45 degrees

Zenith TX2 TAA Endovascular Graft with Pro-Form and the Z-Trak Plus Introduction System - Graft, vascular, synthetic Australia - Inggris - Department of Health (Therapeutic Goods Administration)

zenith tx2 taa endovascular graft with pro-form and the z-trak plus introduction system - graft, vascular, synthetic

william a cook australia pty ltd - 35281 - graft, vascular, synthetic - a two-piece cylindrical endovascular graft consisting of proximal & distal components, constructed of woven polyester sewn to self-expanding z-stents. fully stented to provide stability and the expansile force to open the lumen of the graft during deployment. z-stents also provide attachment/seal of the graft to the vessel wall. barbs used for added fixation. radiopaque gold markers facilitate fluoroscopic visualisation. shipped preloaded onto either a 20fr or 22fr z-trak plus intro. system. intended for treatment of patients with atherosclerotic aneurysms, symptomatic acute or chronic dissections, contained ruptures, growing aneurysms and/or resulting in distal ischaemia, in the descending thoracic aorta having vascular morphology suitable for endovascular repair.

Zenith Universal Distal Body Endovascular Graft - Graft, vascular, synthetic Australia - Inggris - Department of Health (Therapeutic Goods Administration)

zenith universal distal body endovascular graft - graft, vascular, synthetic

william a cook australia pty ltd - 35281 - graft, vascular, synthetic - the zenith universal distal body implant is a bifurcated endovascular graft with one long ipsilateral iliac limb and one short contralateral iliac limb. it is intended to work as a modular system in combination with other zenith proximal devices and iliac leg grafts. the graft is shipped loaded onto the h&l-b one-shot introduction system. it has a sequential deployment method with built-in features to provide continuous control of the graft throughout the deployment procedure. the zenith universal distal body endovascular graft is indicated for the endovascular treatment of patients with abdominal or thoracoabdominal aortic aneurysms, when used with the appropriate zenith proximal device and zenith iliac leg grafts. the patient must have anatomy suitable for endovascular repair, including: ? adequate femoral/iliac access compatible with the required delivery systems; ? an appropriate length of abdominal aorta, distal from the most proximal point of the overlap with the proximal piece to the aortic bifurcation.