Австралия - английски - Department of Health (Therapeutic Goods Administration)

abbott vascular division of abbott medical australia pty ltd - 35094 - catheter guide wire - a coiled wire that is designed to fit inside a percutaneous catheter. it is typically made of stainless steel, with microglide coating (to facilitate movement in the vessels). the device is single-use. all hi-torque guide wires are intended to facilitate the placement of balloon dilatation catheters during percutaneous transluminal coronary angioplasty (ptca) and percutaneous transluminal angioplasty (pta).

Австралия - английски - Department of Health (Therapeutic Goods Administration)

abbott vascular division of abbott medical australia pty ltd - 35094 - catheter guide wire - these guidewires are designed to provide improved torque response and crossing while maintaining tactile feedback in stenotic vessels. the stainless steel core runs through the entire length of the wire. all wires have maximum diameter of 0.0140" and are provided in 190cm extendable and 300cm exchangeable lengths. the distal core segment of this guide wire is offered in 5 configurations. each configuration is identical in design except for those design features that impact tip flexibility. the hi-torque winn guide wire is intended to facilitate the placement of balloon dilatation catheters during percutaneous transluminal coronary angioplasty (ptca) and percutaneous transluminal angioplasty (pta). the guide wire may also be used with compatible stent devices during therapeutic procedures. this is a single use device.

Австралия - английски - Department of Health (Therapeutic Goods Administration)

abbott vascular division of abbott medical australia pty ltd - 47135 - intravascular catheter guidewire extension - a stiff but flexible wire used to extend a compatible vascular guidewire to facilitate the exchange of a catheter, or other interventional device, without exchanging the guidewire, and to maintain the intravascular position of the guidewire, during an interventional procedure in the coronary or peripheral arteries. it is joined to the proximal end of the guidewire with a compatible connector to create the extension. this is a single-use device.

Австралия - английски - Department of Health (Therapeutic Goods Administration)

abbott vascular division of abbott medical australia pty ltd - 12534 - micromanipulator - medical devices used to manipulate other devices in a more precise manner

Австралия - английски - Department of Health (Therapeutic Goods Administration)

abbott vascular division of abbott medical australia pty ltd - 34179 - stent, vascular, coronary artery - balloon expandable stent, supplied encased in a protective sheath, pre-mounted on a balloon dilatation catheter (stent delivery system)is delivered and deployed via inflation of the balloon at the site of the target lesion. using the flushing tool, the guide wire lumen is flushed before use. two radiopaque markers, located underneath the balloon, are used to fluoroscopically position the stent across the lesion. the multi-link 8 coronary stent system is indicated for improving coronary luminal diameter in the following: ? patients with symptomatic ischemic heart disease due to discrete de novo native coronary artery lesions (length = 25 mm) with reference vessel diameters from 2.5 mm to 4.0 mm. ? restoring coronary flow in patients experiencing acute myocardial infarction, who within 12 hours of symptom onset present with native coronary artery lesions (length = 25 mm) with reference vessel diameters from 2.5 mm to 4.0 mm. ? patients with symptomatic ischemic heart disease due to lesions in saphenous vein byp

Австралия - английски - Department of Health (Therapeutic Goods Administration)

abbott vascular division of abbott medical australia pty ltd - 34179 - stent, vascular, coronary artery - balloon expandable stent, supplied encased in a protective sheath, pre-mounted on a balloon dilatation catheter (stent delivery system)is delivered and deployed via inflation of the balloon at the site of the target lesion. using the flushing tool, the guide wire lumen is flushed before use. two radiopaque markers, located underneath the balloon, are used to fluoroscopically position the stent across the lesion. the multi-link 8 ll coronary stent system is indicated for improving coronary luminal diameter in the following: ? patients with symptomatic ischemic heart disease due to discrete de novo native coronary artery lesions (length = 35 mm) with reference vessel diameters from 2.5 mm to 4.0 mm. ? restoring coronary flow in patients experiencing acute myocardial infarction, who within 12 hours of symptom onset present with native coronary artery lesions (length = 35 mm) with reference vessel diameters from 2.5 mm to 4.0 mm. ? patients with symptomatic ischemic heart disease due to lesions in saphenous vein

Австралия - английски - Department of Health (Therapeutic Goods Administration)

abbott vascular division of abbott medical australia pty ltd - 34179 - stent, vascular, coronary artery - delivery to and deployment of a pre-mounted l-605 cocr, balloon expandable stent at the target lesion. radiopaque markers, located underneath the balloon, are utilized to position stent across the lesion. the multi-link 8 sv coronary stent system is indicated for improving coronary luminal diameter in the following: patients with abrupt or threatened abrupt closure with failed interventional therapy of de novo and restenotic native coronary artery lesions (length = 25 mm) with reference vessel diameters from 2.0 mm to 2.5 mm. patients with symptomatic ischemic heart disease due to discrete de novo native coronary artery lesions (length = 25 mm) with reference vessel diameters from 2.25 mm to 2.5 mm.

Австралия - английски - Department of Health (Therapeutic Goods Administration)

abbott vascular division of abbott medical australia pty ltd - 34179 - stent, vascular, coronary artery - a premounted l 605 cobalt chromium alloy stent. two radiopaque markers located underneath the balloon, which fluoroscopically mark the balloon and expanded stent length improving coronary luminal diameter in patients with abrupt or threatened abrupt closure with failed interventional therapy of de nobo and restenotic native coronary artery lesions with diameters of 2.0 to 2.5 mm.

Австралия - английски - Department of Health (Therapeutic Goods Administration)

abbott vascular division of abbott medical australia pty ltd - 34179 - stent, vascular, coronary artery - a pre-mounted l-605 cobalt chromium alloy stent. two radiopaque markeres, located underneath the balloon which fluoroscopically mark the working length of the balloon and the expanded stent. the coronary stent systems are indicated for improving coronary luminal diameter in patients with symptomatic ischaemic heart disease due to discrete de novo native coronary artery lesions (length < 26mm) with reference vessel diameters ranging from 2.75mm to 4.0mm and for restoring coronary flow in patients experiencing acute myocardial infarction who within 12 hours of symptom onset present with native coronary artery lesions of < 26mm in length and a reference vessel diameter of 3.0mm to 4.0mm.

Австралия - английски - Department of Health (Therapeutic Goods Administration)

abbott vascular division of abbott medical australia pty ltd - 17184 - catheter, angioplasty, balloon dilatation - the catheter has an integrated shaft that has a combination single lumen and dual lumen tubing. one lumen is used for the inflation of the balloon with contrast medium. the second lumen allows facilitation advancement of the dilatation catheter to and through the stenosis to be dilated. the balloon radiopaque marker(s) aid in positioning the balloon in the stenosis. the proximal shaft markers aid in gauging dilatation catheter position relative to the guiding catheter tip. the nc trek rx coronary dilatation catheter is indicated for: a) balloon dilatation of the stenotic portion of a coronary artery or bypass graft stenosis, for the purpose of improving myocardial perfusion b) balloon dilatation of a coronary artery occlusion, for the purpose of restoring coronary flow in patients with st-segment elevation myocardial infarction c) balloon dilatation of a stent after implantation