Ex parte ESROCK - Page 5




               Appeal No. 2000-1763                                                                        Page 5                 
               Application No. 09/227,037                                                                                         


                              A disposable tubular device of the present invention (e.g., the syringe tip                         
                      24) is preferably made by a dual-extrusion method.  A first material is  extruded                           
                      through a first die to form an inner tube 36.  This die is configured such that                             
                      extrusion of the first material through the first die forms an elongate tube with                           
                      elongate flutes.  The flutes extend along substantially the entire length of the                            
                      tube.  The fluted tube is then passed longitudinally through a second die while a                           
                      second material is extruded through the second die and around the inner tube.                               
                      The extruded tubes are then cut to length to form the tip 24.  The second die is                            
                      configured so that the outer tube 38 (sleeve) so formed fits snugly over the inner                          
                      tube 36.  The sleeve 38 constitutes a tube-support structure for maintaining the                            
                      general overall shape of the inner tube 36.  The flutes 46 and a portion of an                              
                      inner surface 50 of the sleeve 38 define a plurality of fluid passageways 52.  The                          
                      first and second materials are selected so that the outer tube of the tip 24 is stiffer                     
                      than the inner tube at the typical operating temperatures of the syringe (e.g.,                             
                      temperatures in the range of 50  F. to 110   F.).o         o                                                               

                      We have carefully reviewed the appellant's specification, paying special attention to the                   
               above-mentioned portions alluded to by the examiner, but we perceive therefrom no indication                       
               that extrusion of a first material through a first die to form the tube and movement of the tube                   
               through a second die while a second material is extruded through the second die to form the                        
               tube-support structure is critical to the invention.  As we see it, the critical features of the                   
               invention are the steps of forming an inner tube of a first pliable, resilient material adapted to                 
               form a fluid-tight seal with a medical instrument and forming a tube-support structure (outer                      
               tube) having a stiffness and hardness greater than that of the inner tube so as to make a tubular                  
               structure capable of releasable and sealing connection to a medical instrument.  As pointed out                    
               in column 3, lines 33-38, of the appellant's specification, the inner tube and outer tube                          
               preferably are held together by a close friction fit or, alternatively, may be bonded together by                  









Page:  Previous  1  2  3  4  5  6  7  8  9  10  11  12  Next 

Last modified: November 3, 2007