Abstract: An over-the-needle catheter assembly includes a tube made of a flexible, biocompatible material. The tube has a proximal portion, a distal portion and a catheter tip positioned on the distal portion remote from the proximal portion. A lumen extends through the tube, substantially co-axially with the tube, from the proximal portion, through the distal portion and through to the catheter tip. The lumen cross-section at the proximal portion is larger than the cross-section at the distal portion. A shoulder is disposed in the lumen between the distal portion and the proximate portion. A catheter land, having a predetermined length, is defined as the portion of the lumen disposed in the distal portion of the tube between the shoulder and the distal end. A needle is disposed in the lumen and has a substantially circular cross-section. A discontinuity is located on the needle at a predetermined position with respect to the needle tip.

Abstract: An over-the-needle catheter assembly includes a tube made of a flexible, biocompatible material. The tube has a proximal portion, a distal portion and a catheter tip positioned on the distal portion remote from the proximal portion. A lumen extends through the tube, substantially co-axially with the tube, from the proximal portion, through the distal portion and through to the catheter tip. The lumen cross-section at the proximal portion is larger than the cross-section at the distal portion. A shoulder is disposed in the lumen between the distal portion and the proximate portion. A catheter land, having a predetermined length, is defined as the portion of the lumen disposed in the distal portion of the tube between the shoulder and the distal end. A needle is disposed in the lumen and has a substantially circular cross-section. A discontinuity is located on the needle at a predetermined position with respect to the needle tip.

Abstract: An over-the-needle catheter assembly includes a tube made of a flexible, biocompatible material. The tube has a proximal portion, a distal portion and a catheter tip positioned on the distal portion remote from the proximal portion. A lumen extends through the tube, substantially co-axially with the tube, from the proximal portion, through the distal portion and through to the catheter tip. The lumen cross-section at the proximal portion is larger than the cross-section at the distal portion. A shoulder is disposed in the lumen between the distal portion and the proximate portion. A catheter land, having a predetermined length, is defined as the portion of the lumen disposed in the distal portion of the tube between the shoulder and the distal end. A needle is disposed in the lumen and has a substantially circular cross-section. A discontinuity is located on the needle at a predetermined position with respect to the needle tip.

Abstract: This invention relates to a splittable medical device incorporating two sets of preferential tear lines. The first set of preferential tear lines preferably includes two longitudinally extending skives formed along the exterior surface of the proximal portion of the splittable medical device. The second set of preferential tear lines preferably includes a plurality of grooves formed along a distal portion of the interior portion of the splittable medical device. The skives should be substantially aligned with some of the grooves. This configuration facilitates splitting of the medical device along the skives and along one or more of the grooves to allow a clinician to split the medical device completely into two pieces. This invention includes a special mandrel having a plurality of ribs formed along a distal portion thereof and process that is used to manufacture the splittable medical device.

Abstract: This invention relates to a splittable medical device incorporating two sets of preferential tear lines. The first set of preferential tear lines preferably includes two longitudinally extending skives formed along the exterior surface of the proximal portion of the splittable medical device. The second set of preferential tear lines preferably includes a plurality of grooves formed along a distal portion of the interior portion of the splittable medical device. The skives should be substantially aligned with some of the grooves. This configuration facilitates splitting of the medical device along the skives and along one or more of the grooves to allow a clinician to split the medical device completely into two pieces. This invention includes a special mandrel having a plurality of ribs formed along a distal portion thereof and process that is used to manufacture the splittable medical device.