IP Library Granted Patent US 7,536,226
Granted Patent B2
US 7,536,226 · App. 10/492,578 · Granted May 19, 2009

Electro-nerve stimulator system and methods

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Quick Facts
Patent No.
US 7,536,226
App. No.
10/492,578
Granted
May 19, 2009
Kind
B2
Abstract

An electro-nerve stimulation apparatus includes a pulse generator, a first electrically conductive, insulated lead wire, a second electrically conductive, insulated lead wire, an electrically conductive transcutaneous electrode and an electrically conductive percutaneous needle electrode. Connected to one end of the first and second lead wires is a connector for electrically coupling with the pulse generator. The transcutaneous electrode is operably connected to the other end of the first lead wire. An electrically conductive adaptor is secured to the other end of the second lead wire for electrically coupling to the terminal end of the percutaneous needle electrode. The lead wire set includes a single-use mechanism adapted to effectively discourage reuse of the electrodes. In use, the transcutaneous electrode is adhered to the patient's skin distal from the desired internal stimulation site. The percutaneous needle electrode is inserted through the skin in proximity to the desired internal stimulation site. The pulse generator is activated to pass current pulses between the transcutaneous electrode and the percutaneous needle electrode through the internal stimulation site.

Claims (158)

1. An electro-nerve stimulation apparatus, comprising:

a pulse generator for generating electrical pulses, said pulse generator having a first lead wire interface and a second lead wire interface;

a percutaneous needle electrode; and

a lead wire set removably connectable to the pulse generator and comprising;

a first electrically conductive, insulated lead wire having first and second ends, said first end of said first lead wire comprising a first connector for electrically coupling with said first lead wire interface of said pulse generator, said second end of said first lead wire operably comprising an electrically conductive transcutaneous electrode for delivering electrical pulses generated by the pulse generator to a patient's skin;

a second electrically conductive, insulated lead wire having first and second ends, said first end of said second lead wire comprising a second connector for electrically coupling with said second lead wire interface of said pulse generator, said second end of said second lead wire comprising an electrically conductive and mechanically suspendable attachment member for being suspended by and electrically connecting with said percutaneous needle electrode; and

a single-use mechanism comprising a part of said lead wire set to effectively discourage re-use thereof;

wherein said attachment member includes an electrically conductive tape member having an adhesive portion;

wherein a terminal end of said percutaneous needle electrode is fixedly adhered to said adhesive portion of said electrically conductive tape member, whereby said percutaneous needle electrode is not readily removable therefrom without damaging said tape member; and

wherein said electrically conductive tape member further includes a non-adhesive electrically conductive portion for testing proper placement of said other end of said percutaneous needle electrode in proximity to said internal stimulation site prior to adhering said terminal end of said percutaneous needle electrode to said adhesive portion of said electrically conductive tape member.

2. The apparatus of claim 1 , wherein said electrically conductive transcutaneous electrode includes adhesive on a face thereof for removably securing said transcutaneous electrode onto said patient's body at a desired location.

3. The apparatus of claim 2 , wherein said adhesive on said face of said transcutaneous electrode is a single-use adhesive such that upon removal of said transcutaneous electrode from said patient's skin said adhesive will not readily readhere to said patient's skin.

4. An electro-nerve stimulation apparatus, comprising:

a pulse generator for generating electrical pulses, said pulse generator having a first lead wire interface and a second lead wire interface;

a first electrically conductive, insulated lead wire having first and second ends, said first end of said first lead wire fixedly secured to a first connector for electrically coupling with said first lead wire interface of said pulse generator, said second end of said first lead wire operably secured to an electrically conductive transcutaneous electrode for delivering electrical pulses generated by the pulse generator to a patient's skin;

a second electrically conductive, insulated lead wire having first and second ends, said first end of said second lead wire fixedly secured to a second connector for electrically coupling with said second lead wire interface of said pulse generator, said second end of said second lead wire fixedly secured to an electrically conductive adaptor for electrically connecting with a terminal end of a percutaneous needle electrode; and

a single male connector comprising said first and second connectors fixedly secured to said first ends of said first and second lead wires;

wherein said pulse generator includes a single mating female receptacle for electrically coupling said first and second lead wires with said first and second lead wire interfaces; and

wherein said single male connector is a single-use connector whereby said single male connector is not readily reusable to effectively discourage re-use of the percutaneous and transcutaneous electrodes.

5. The apparatus of claim 4 , wherein said single male connector and said single mating female receptacle are keyed to ensure proper orientation and electrical coupling of said first and second lead wires with the respective first and second lead wire interfaces of said pulse generator.

6. The apparatus of claim 4 wherein said single use connector includes a fuse adapted to burn out after a preselected time period.

7. The apparatus of claim 4 wherein said single use connector includes an EPROM programmed to prevent electrical connection of said first and second lead wires with said first and second lead wire interfaces.

8. The apparatus of claim 4 wherein said single use connector includes a fuse and an EPROM programmed to burn out said fuse after a predetermined time period.

9. The apparatus of claim 4 wherein said single use connector includes a fuse and an EPROM programmed to generate a current spike to burn out said fuse after a predetermined time period.

10. An electro-nerve stimulation apparatus, comprising:

a pulse generator for generating electrical pulses, said pulse generator having a first lead wire interface and a second lead wire interface;

a percutaneous needle electrode; and

a lead wire set removably connectable to the pulse generator and comprising:

a first electrically conductive, insulated lead wire having first and second ends, said first end of said first lead wire comprising a first connector for electrically coupling with said first lead wire interface of said pulse generator, said second end of said first lead wire operably comprising an electrically conductive transcutaneous electrode for delivering electrical pulses generated by the pulse generator to a patient's skin;

a second electrically conductive, insulated lead wire having first and second ends, said first end of said second lead wire comprising a second connector for electrically coupling with said second lead wire interface of said pulse generator, said second end of said second lead wire comprising an electrically conductive and mechanically suspendable attachment member for being suspended by and electrically connecting with said percutaneous needle electrode; and

a single-use mechanism comprising a part of said lead wire set to effectively discourage re-use thereof;

wherein said attachment member includes a clip having an electrically conductive bridge member movable between a first open position and a second closed position;

wherein a terminal end of said percutaneous needle electrode is secured to said electrically conductive bridge member;

wherein said clip is a single-use clip; and

wherein said bridge member fails after a predetermined time period of current pulses traverse therethrough.

11. An electro-nerve stimulation apparatus, comprising:

a pulse generator for generating electrical pulses, said pulse generator having a first lead wire interface and a second lead wire interface;

a percutaneous needle electrode; and

a lead wire set removably connectable to the pulse generator and comprising:

a first electrically conductive, insulated lead wire having first and second ends, said first end of said first lead wire comprising a first connector for electrically coupling with said first lead wire interface of said pulse generator, said second end of said first lead wire operably comprising an electrically conductive transcutaneous electrode for delivering electrical pulses generated by the pulse generator to a patient's skin;

a second electrically conductive, insulated lead wire having first and second ends, said first end of said second lead wire comprising a second connector for electrically coupling with said second lead wire interface of said pulse generator, said second end of said second lead wire comprising an electrically conductive and mechanically suspendable attachment member for being suspended by and electrically connecting with said percutaneous needle electrode; and

a single-use mechanism comprising a part of said lead wire set to effectively discourage re-use thereof;

wherein said attachment member includes a clip having an electrically conductive bridge member movable between a first open position and a second closed position;

wherein a terminal end of said percutaneous needle electrode is secured to said electrically conductive bridge member;

wherein said clip is a single-use clip; and

wherein said bridge member welds to said terminal end of said percutaneous needle electrode after a predetermined time period of current pulses traverse therethrough.

12. An electro-nerve stimulation apparatus, comprising:

a pulse generator for generating electrical pulses, said pulse generator having a first lead wire interface and a second lead wire interface;

a single male connector; and

a lead wire set removably connectable to the pulse generator and comprising;

a first electrically conductive, insulated lead wire having first and second ends, said first end of said first lead wire comprising a first connector for electrically coupling with said first lead wire interface of said pulse generator, said second end of said first lead wire operably comprising an electrically conductive transcutaneous electrode for delivering electrical pulses generated by the pulse generator to a patient's skin;

a second electrically conductive, insulated lead wire having first and second ends, said first end of said second lead wire comprising a second connector for electrically coupling with said second lead wire interface of said pulse generator, said second end of said second lead wire comprising an electrically conductive and mechanically suspendable attachment member for being suspended by and electrically connecting with a percutaneous needle electrode; and

a single-use mechanism comprising a part of said lead wire set to effectively discourage re-use thereof;

wherein said attachment member includes a clip having an electrically conductive bridge member movable between a first open position and a second closed position;

wherein the single male conductor comprises said first and second connectors fixedly secured to said first ends of said first and second lead wires;

wherein said pulse generator includes a single mating female receptacle for electrically coupling said first and second lead wires with said first and second lead wire interfaces; and

wherein said single male connector and said mating single female receptacle are keyed to ensure proper orientation and electrical coupling of said first and second lead wires only with the respective first and second lead wire interfaces of said pulse generator.

13. The apparatus of claim 12 , wherein said single male connector is a single-use connector whereby said single male connector is not readily reusable.

14. The apparatus of claim 13 wherein said single use connector includes a fuse adapted to burn out after a preselected time period.

15. The apparatus of claim 13 wherein said single use connector includes an EPROM programmed to prevent electrical connection of said first and second lead wires with said first and second lead wire interfaces.

16. The apparatus of claim 13 wherein said single use connector includes a fuse and an EPROM programmed to burn out said fuse after a predetermined time period.

17. The apparatus of claim 13 wherein said single use connector includes a fuse and an EPROM programmed to generate a current spike to burn out said fuse after a predetermined time period.

18. A method for electro-nerve stimulation, comprising the steps of:

providing a pulse generator for generating electrical pulses, said pulse generator having a first lead wire interface and a second lead wire interface;

providing a removably connectable lead wire set for the pulse generator; providing the lead wire set with a first electrically conductive, insulated lead wire having first and second ends, said first end of said first lead wire comprising a connector for electrically coupling with said first lead wire interface of said pulse generator, said second end of said first lead wire operably comprising an electrically conductive transcutaneous electrode for delivering electrical pulses generated by said pulse generator to a patient's skin;

providing an electrically conductive percutaneous needle electrode, said electrically conductive percutaneous needle electrode having one end insertable into a patient's body in proximity to a preselected internal stimulation site to receive electrical pulses from said transcutaneous electrode;

providing the lead wire set with a second electrically conductive, insulated lead wire having first and second ends, said first end of said second lead wire comprising a connector for electrically coupling with said second lead wire interface of said pulse generator, said second end of said second lead wire comprising an electrically conductive and mechanically suspendable attachment member;

providing the lead wire set with a single-use mechanism to effectively discourage re-use thereof;

penetrating said patient's skin with said one end of said percutaneous needle electrode and advancing said one end into proximity with said preselected internal stimulation site;

electrically connecting a terminal end of said percutaneous needle electrode to said attachment member;

adhering said transcutaneous electrode onto said patient's skin distal to said preselected internal stimulation site;

electrically coupling said first and second lead wires with said respective first and second lead wire interfaces of said pulse generator; and

activating said pulse generator to generate electrical pulses that traverse the preselected internal stimulation site between said transcutaneous electrode and said percutaneous needle electrode;

wherein said electrically conductive transcutaneous electrode includes adhesive on a face thereof for removably securing said electrode onto said skin of said patient; and

wherein said adhesive on said face of said transcutaneous electrode is a single-use adhesive such that upon removal of said transcutaneous electrode from said patient's skin said adhesive will not readily re-adhere to said patient's skin.

19. A method for electro-nerve stimulation, comprising the steps of:

providing a pulse generator for generating electrical pulses, said pulse generator having a first lead wire interface and a second lead wire interface;

providing a removably connectable lead wire set for the pulse generator;

providing the lead wire set with a first electrically conductive, insulated lead wire having first and second ends, said first end of said first lead wire comprising a connector for electrically coupling with said first lead wire interface of said pulse generator, said second end of said first lead wire operably comprising an electrically conductive transcutaneous electrode for delivering electrical pulses generated by said pulse generator to a patient's skin;

providing an electrically conductive percutaneous needle electrode, said electrically conductive percutaneous needle electrode having one end insertable into a patient's body in proximity to a preselected internal stimulation site to receive electrical pulses from said transcutaneous electrode;

providing the lead wire set with a second electrically conductive, insulated lead wire having first and second ends, said first end of said second lead wire comprising a connector for electrically coupling with said second lead wire interface of said pulse generator, said second end of said second lead wire comprising an electrically conductive and mechanically suspendable attachment member;

providing the lead wire set with a single-use mechanism to effectively discourage re-use thereof;

penetrating said patient's skin with said one end of said percutaneous needle electrode and advancing said one end into proximity with said preselected internal stimulation site;

electrically connecting a terminal end of said percutaneous needle electrode to said attachment member;

adhering said transcutaneous electrode onto said patient's skin distal to said preselected internal stimulation site;

electrically coupling said first and second lead wires with said respective first and second lead wire interfaces of said pulse generator; and

activating said pulse generator to generate electrical pulses that traverse the preselected internal stimulation site between said transcutaneous electrode and said percutaneous needle electrode;

wherein said attachment member includes an electrically conductive tape member having an adhesive portion; and

wherein said step of connecting said terminal end of said percutaneous needle electrode to said attachment member includes the step of fixedly adhering said adhesive portion of said electrically conductive tape member to said terminal end, whereby said percutaneous needle electrode is not readily removable therefrom without damaging said tape member;

further including the step of testing proper placement of said one end of said percutaneous needle electrode in proximity to said preselected internal stimulation site prior to fixedly adhering said terminal end of said percutaneous needle electrode to said adhesive portion of said electrically conductive tape member by contacting said other end of said percutaneous needle with a non-adhesive electrically conductive portion of said electrically conductive tape member.

20. A method for electro-nerve stimulation, comprising the steps of:

providing a pulse generator for generating electrical pulses, said pulse generator having a first lead wire interface and a second lead wire interface;

providing a first electrically conductive, insulated lead wire having first and second ends, said first end of said first lead wire fixedly secured to a connector for electrically coupling with said first lead wire interface of said pulse generator, said second end of said first lead wire operably secured to an electrically conductive transcutaneous electrode for delivering electrical pulses generated by said pulse generator to a patient's skin;

providing an electrically conductive percutaneous needle electrode, said electrically conductive percutaneous needle electrode having one end insertable into a patient's body in proximity to a preselected internal stimulation site to receive electrical pulses from said transcutaneous electrode;

providing a second electrically conductive, insulated lead wire having first and second ends, said first end of said second lead wire fixedly secured to a connector for electrically coupling with said second lead wire interface of said pulse generator, said second end of said second lead wire fixedly secured to an electrically conductive adaptor;

penetrating said patient's skin with said one end of said percutaneous needle electrode and advancing said one end into proximity with said preselected internal stimulation site;

electrically connecting a terminal end of said percutaneous needle electrode to said electrically conductive single-use adaptor;

adhering said transcutaneous electrode onto said patient's skin distal to said preselected internal stimulation site;

electrically coupling said first and second lead wires with said respective first and second lead wire interfaces of said pulse generator; and

activating said pulse generator to generate electrical pulses that traverse the preselected internal stimulation site between said transcutaneous electrode and said percutaneous needle electrode;

wherein said first and second connectors fixedly secured to said first ends of said first and second lead wires comprise a single male connector;

wherein said pulse generator includes a single mating female receptacle for electrically coupling said first and second lead wires with said first and second lead wire interfaces; and

wherein said single male connector is a single-use connector whereby said single male connector is not readily reusable to effectively discourage re-use of said percutaneous and transcutaneous electrodes.

21. The method of claim 20 , wherein said single male connector and said mating single female receptacle are keyed to ensure proper orientation and electrical coupling of said first and second lead wires with the respective first and second lead wire interfaces of said pulse generator.

22. The method of claim 20 wherein said single use connector includes a fuse adapted to burn out after a preselected time period.

23. The method of claim 20 wherein said single use connector includes an EPROM programmed to prevent electrical connection of said first and second lead wires with said first and second lead wire interfaces.

24. The method of claim 20 wherein said single use connector includes a fuse and an EPROM programmed to burn out said fuse after a predetermined time period.

25. The method of claim 20 wherein said single use connector includes a fuse and an EPROM programmed to generate a current spike to burn out said fuse after a predetermined time period.

26. A method for electro-nerve stimulation, comprising the steps of:

providing a pulse generator for generating electrical pulses, said pulse generator having a first lead wire interface and a second lead wire interface;

providing a removably connectable lead wire set for the pulse generator;

providing the lead wire set with a first electrically conductive, insulated lead wire having first and second ends, said first end of said first lead wire comprising a connector for electrically coupling with said first lead wire interface of said pulse generator, said second end of said first lead wire operably comprising an electrically conductive transcutaneous electrode for delivering electrical pulses generated by said pulse generator to a patient's skin;

providing an electrically conductive percutaneous needle electrode, said electrically conductive percutaneous needle electrode having one end insertable into a patient's body in proximity to a preselected internal stimulation site to receive electrical pulses from said transcutaneous electrode;

providing the lead wire set with a second electrically conductive, insulated lead wire having first and second ends, said first end of said second lead wire comprising a connector for electrically coupling with said second lead wire interface of said pulse generator, said second end of said second lead wire comprising an electrically conductive and mechanically suspendable attachment member;

providing the lead wire set with a single-use mechanism to effectively discourage re-use thereof;

penetrating said patient's skin with said one end of said percutaneous needle electrode and advancing said one end into proximity with said preselected internal stimulation site;

electrically connecting a terminal end of said percutaneous needle electrode to said attachment member;

adhering said transcutaneous electrode onto said patient's skin distal to said preselected internal stimulation site;

electrically coupling said first and second lead wires with said respective first and second lead wire interfaces of said pulse generator; and

activating said pulse generator to generate electrical pulses that traverse the preselected internal stimulation site between said transcutaneous electrode and said percutaneous needle electrode;

wherein said attachment member includes a clip having an electrically conductive bridge member movable between a first open position and a second closed position;

wherein said step of connecting said terminal end of said percutaneous needle electrode to said attachment member includes the step of connecting said terminal end of said percutaneous needle electrode to said electrically conductive bridge member;

wherein said clip is a single-use clip; and

wherein said bridge member fails after a predetermined time period of current pulses traverse therethrough.

27. A method for electro-nerve stimulation, comprising the steps of:

providing a pulse generator for generating electrical pulses, said pulse generator having a first lead wire interface and a second lead wire interface;

providing a removably connectable lead wire set for the pulse generator;

providing the lead wire set with a first electrically conductive, insulated lead wire having first and second ends, said first end of said first lead wire comprising a connector for electrically coupling with said first lead wire interface of said pulse generator, said second end of said first lead wire operably comprising an electrically conductive transcutaneous electrode for delivering electrical pulses generated by said pulse generator to a patient's skin;

providing an electrically conductive percutaneous needle electrode, said electrically conductive percutaneous needle electrode having one end insertable into a patient's body in proximity to a preselected internal stimulation site to receive electrical pulses from said transcutaneous electrode;

providing the lead wire set with a second electrically conductive, insulated lead wire having first and second ends, said first end of said second lead wire comprising a connector for electrically coupling with said second lead wire interface of said pulse generator, said second end of said second lead wire comprising an electrically conductive and mechanically suspendable attachment member;

providing the lead wire set with a single-use mechanism to effectively discourage re-use thereof;

penetrating said patient's skin with said one end of said percutaneous needle electrode and advancing said one end into proximity with said preselected internal stimulation site;

electrically connecting a terminal end of said percutaneous needle electrode to said attachment member;

adhering said transcutaneous electrode onto said patient's skin distal to said preselected internal stimulation site;

electrically coupling said first and second lead wires with said respective first and second lead wire interfaces of said pulse generator; and

activating said pulse generator to generate electrical pulses that traverse the preselected internal stimulation site between said transcutaneous electrode and said percutaneous needle electrode;

wherein said attachment member includes a clip having an electrically conductive bridge member movable between a first open position and a second closed position;

wherein said step of connecting said terminal end of said percutaneous needle electrode to said attachment member includes the step of connecting said terminal end of said percutaneous needle electrode to said electrically conductive bridge member;

wherein said clip is a single-use clip; and

wherein said bridge member welds to said terminal end of said percutaneous needle electrode after a predetermined time period of current pulses traverse therethrough.

28. A method for electro-nerve stimulation, comprising the steps of:

providing a pulse generator for generating electrical pulses, said pulse generator having a first lead wire interface and a second lead wire interface;

providing a removably connectable lead wire set for the pulse generator;

providing the lead wire set with a first electrically conductive, insulated lead wire having first and second ends, said first end of said first lead wire comprising a connector for electrically coupling with said first lead wire interface of said pulse generator, said second end of said first lead wire operably comprising an electrically conductive transcutaneous electrode for delivering electrical pulses generated by said pulse generator to a patient's skin;

providing an electrically conductive percutaneous needle electrode, said electrically conductive percutaneous needle electrode having one end insertable into a patient's body in proximity to a preselected internal stimulation site to receive electrical pulses from said transcutaneous electrode;

providing the lead wire set with a second electrically conductive, insulated lead wire having first and second ends, said first end of said second lead wire comprising a connector for electrically coupling with said second lead wire interface of said pulse generator, said second end of said second lead wire comprising an electrically conductive and mechanically suspendable attachment member;

providing the lead wire set with a single-use mechanism to effectively discourage re-use thereof;

penetrating said patient's skin with said one end of said percutaneous needle electrode and advancing said one end into proximity with said preselected internal stimulation site;

electrically connecting a terminal end of said percutaneous needle electrode to said attachment member;

adhering said transcutaneous electrode onto said patient's skin distal to said preselected internal stimulation site;

electrically coupling said first and second lead wires with said respective first and second lead wire interfaces of said pulse generator; and

activating said pulse generator to generate electrical pulses that traverse the preselected internal stimulation site between said transcutaneous electrode and said percutaneous needle electrode;

wherein said attachment member includes a clip having an electrically conductive bridge member movable between a first open position and a second closed position; and

wherein said first and second connectors fixedly secured to said first ends of said first and second lead wires comprise a single male connector and wherein said pulse generator includes a single mating female receptacle for electrically coupling said first and second lead wires with said first and second lead wire interfaces, and further wherein said single male connector and said mating single female receptacle are keyed to ensure proper orientation and electrical coupling of said first and second lead wires only with the respective first and second lead wire interfaces of said pulse generator.

29. The method of claim 28 , wherein said single male connector is a single-use connector whereby said single male connector is not readily reusable.

30. The method of claim 29 wherein said single use connector includes a fuse adapted to burn out after a preselected time period.

31. The method of claim 29 wherein said single use connector includes an EPROM programmed to prevent electrical connection of said first and second lead wires with said first and second lead wire interfaces.

32. The method of claim 29 wherein said single use connector includes a fuse and an EPROM programmed to burn out said fuse after a predetermined time period.

Assignments (12)
RELEASE OF SECURITY INTEREST IN PATENTS Recorded Feb 12, 2020
From: JPMORGAN CHASE BANK, N.A. AS ADMINISTRATIVE AGENT
To: COGENTIX MEDICAL, INC.; LABORIE MEDICAL TECHNOLOGIES CANADA ULC; UROPLASTY LLC
Reel/Frame 051906/0518 →
SECURITY INTEREST Recorded Apr 23, 2018
From: COGENTIX MEDICAL, INC.; UROPLASTY LLC; LABORIE MEDICAL TECHNOLOGIES CANADA ULC
To: JPMORGAN CHASE BANK, N.A.
Reel/Frame 045609/0561 →
MERGER AND CHANGE OF NAME Recorded Apr 16, 2015
From: UROPLASTY, INC.; VISOR MERGER SUB LLC
To: UROPLASTY, LLC
Reel/Frame 035426/0303 →
CORRECTIVE ASSIGNMENT TO CORRECT THE THE EXECUTION DATE OF THE INVENTOR. DOCUMENT PREVIOUSLY RECORDED AT REEL 015250 FRAME 0478. Recorded Mar 23, 2009
From: VAN DEN BIGGELAAR, HANS
To: CYSTOMEDIX, INC.
Reel/Frame 022436/0594 →
CORRECTIVE ASSIGNMENT TO CORRECT THE EXECUTION DATE OF THE ASSIGNOR. DOCUMENT PREVIOUSLY RECORDED AT REEL 015250 FRAME 0476 Recorded Mar 23, 2009
From: VAN AART, FRED
To: CYSTOMEDIX, INC.
Reel/Frame 022436/0654 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 27, 2007
From: CYSTOMEDIX, INC.
To: UROPLASTY, INC.
Reel/Frame 019628/0553 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 15, 2004
From: VAN DEN BIGGELAAR, HANS
To: CYSTOMEDIX, INC.
Reel/Frame 015250/0478 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 15, 2004
From: VAN AART, FRED
To: CYSTOMEDIX, INC.
Reel/Frame 015250/0476 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 26, 2004
From: VAN DEN BIGGELAAR, HANS
To: CYSTOMEDIX, INC.
Reel/Frame 014656/0665 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 26, 2004
From: VAN HELVOIRT, PIET
To: CYSTOMEDIX, INC.
Reel/Frame 014656/0667 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 26, 2004
From: VAN AART, FRED
To: CYSTOMEDIX, INC.
Reel/Frame 014656/0628 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 24, 2004
From: WILLIAMS, JEFFREY M.
To: CYSTOMEDIX, INC.
Reel/Frame 014649/0103 →