Other products from "ST. JUDE MEDICAL CARDIOVASCULAR DIVISION"
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 05414734206679 401980 401980 IKD CABLE, ELECTRODE 2 Supreme™
2 05414734001212 401775 401775 LDF ELECTRODE, PACEMAKER, TEMPORARY 2 Pacel™
3 05414734001236 401776 401776 LDF ELECTRODE, PACEMAKER, TEMPORARY 2 Pacel™
4 05414734001151 401772 401772 LDF ELECTRODE, PACEMAKER, TEMPORARY 2 Pacel™
5 05414734001137 401771 401771 LDF ELECTRODE, PACEMAKER, TEMPORARY 2 Pacel™
6 05414734027281 401769 401769 LDF ELECTRODE, PACEMAKER, TEMPORARY 2 Pacel™
7 05414734026512 401765 401765 LDF ELECTRODE, PACEMAKER, TEMPORARY 2 Pacel™
8 05414734022521 401764 401764 LDF ELECTRODE, PACEMAKER, TEMPORARY 2 Pacel™
9 05414734021906 401761 401761 LDF ELECTRODE, PACEMAKER, TEMPORARY 2 Pacel™
10 05414734007856 401763 401763 LDF ELECTRODE, PACEMAKER, TEMPORARY 2 Pacel™
11 05414734001199 401774 401774 LDF ELECTRODE, PACEMAKER, TEMPORARY 2 Pacel™
12 05414734001175 401773 401773 LDF ELECTRODE, PACEMAKER, TEMPORARY 2 Pacel™
13 05414734001090 401768 401768 LDF ELECTRODE, PACEMAKER, TEMPORARY 2 Pacel™
14 05414734001052 401766 401766 LDF ELECTRODE, PACEMAKER, TEMPORARY 2 Pacel™
15 05414734001045 401762 401762 LDF ELECTRODE, PACEMAKER, TEMPORARY 2 Pacel™
16 05414734202817 402032 402032 DRA,DRF CATHETER, STEERABLE,CATHETER, ELECTRODE RECORDING, OR PROBE, ELECTRODE RECORDING 2 Livewire™
17 05414734202749 401991 401991 DRA,DRF CATHETER, STEERABLE,CATHETER, ELECTRODE RECORDING, OR PROBE, ELECTRODE RECORDING 2 Livewire™
18 05414734202732 401990 401990 DRA,DRF CATHETER, STEERABLE,CATHETER, ELECTRODE RECORDING, OR PROBE, ELECTRODE RECORDING 2 Livewire™
19 05414734202510 401786 401786 Steerable Electrophysiology Catheter DRF,DRA CATHETER, ELECTRODE RECORDING, OR PROBE, ELECTRODE RECORDING,CATHETER, STEERABLE 2 Livewire™
20 05414734202428 401655 401655 DRA,DRF CATHETER, STEERABLE,CATHETER, ELECTRODE RECORDING, OR PROBE, ELECTRODE RECORDING 2 Livewire™
21 05414734202404 401653 401653 DRA,DRF CATHETER, STEERABLE,CATHETER, ELECTRODE RECORDING, OR PROBE, ELECTRODE RECORDING 2 Livewire™
22 05414734202398 401652 401652 DRA CATHETER, STEERABLE 2 Livewire™
23 05414734202251 401582 401582 DRA,DRF CATHETER, STEERABLE,CATHETER, ELECTRODE RECORDING, OR PROBE, ELECTRODE RECORDING 2 Livewire™
24 05414734202244 401581 401581 DRA,DRF CATHETER, STEERABLE,CATHETER, ELECTRODE RECORDING, OR PROBE, ELECTRODE RECORDING 2 Livewire™
25 05414734202237 401580 401580 DRA,DRF CATHETER, STEERABLE,CATHETER, ELECTRODE RECORDING, OR PROBE, ELECTRODE RECORDING 2 Livewire™
26 05414734202183 401575 401575 DRA,DRF CATHETER, STEERABLE,CATHETER, ELECTRODE RECORDING, OR PROBE, ELECTRODE RECORDING 2 Livewire™
27 05414734200325 402274 402274 Bi-Directional Ablation Catheter LPB Cardiac ablation percutaneous catheter 3 Livewire™
28 05414734200318 402273 402273 Bi-Directional Ablation Catheter LPB Cardiac ablation percutaneous catheter 3 Livewire™
29 05414734200301 402271 402271 Bi-Directional Ablation Catheter LPB Cardiac ablation percutaneous catheter 3 Livewire™
30 05414734200295 402208 402208 Ablation Catheter LPB Cardiac ablation percutaneous catheter 3 Livewire™
31 05414734200288 402207 402207 Ablation Catheter LPB Cardiac ablation percutaneous catheter 3 Livewire™
32 05414734200271 402206 402206 Ablation Catheter LPB Cardiac ablation percutaneous catheter 3 Livewire™
33 05414734200257 402152 402152 Ablation Catheter LPB Cardiac ablation percutaneous catheter 3 Livewire™
34 05414734200240 402151 402151 Ablation Catheter LPB Cardiac ablation percutaneous catheter 3 Livewire™
35 05414734200233 402150 402150 Ablation Catheter LPB Cardiac ablation percutaneous catheter 3 Livewire™
36 05414734200226 402149 402149 Ablation Catheter LPB Cardiac ablation percutaneous catheter 3 Livewire™
37 05414734202695 401941 401941 DRA,DRF CATHETER, STEERABLE,CATHETER, ELECTRODE RECORDING, OR PROBE, ELECTRODE RECORDING 2 Livewire™
38 05414734202688 401940 401940 DRA,DRF CATHETER, STEERABLE,CATHETER, ELECTRODE RECORDING, OR PROBE, ELECTRODE RECORDING 2 Livewire™
39 05414734202671 401939 401939 DRA,DRF CATHETER, STEERABLE,CATHETER, ELECTRODE RECORDING, OR PROBE, ELECTRODE RECORDING 2 Livewire™
40 05414734202664 401938 401938 DRA,DRF CATHETER, STEERABLE,CATHETER, ELECTRODE RECORDING, OR PROBE, ELECTRODE RECORDING 2 Livewire™
41 05414734202602 401923 401923 DRA,DRF CATHETER, STEERABLE,CATHETER, ELECTRODE RECORDING, OR PROBE, ELECTRODE RECORDING 2 Livewire™
42 05414734202589 401917 401917 DRA,DRF CATHETER, STEERABLE,CATHETER, ELECTRODE RECORDING, OR PROBE, ELECTRODE RECORDING 2 Livewire™
43 05414734202572 401915 401915 DRA,DRF CATHETER, STEERABLE,CATHETER, ELECTRODE RECORDING, OR PROBE, ELECTRODE RECORDING 2 Livewire™
44 05414734217347 A402580 A402580 LPB Cardiac ablation percutaneous catheter 3 Livewire TC™
45 05414734217323 402518 402518 LPB Cardiac ablation percutaneous catheter 3 Livewire TC™
46 05414734206211 Bi-Directional Variable Radius Catheter D402865 DRF CATHETER, ELECTRODE RECORDING, OR PROBE, ELECTRODE RECORDING 2 Reflexion Spiral™
47 05414734054256 401777 401777 DSA CABLE, TRANSDUCER AND ELECTRODE, PATIENT, (INCLUDING CONNECTOR) 2 SJM™
48 05414734053679 401760 401760 DSA CABLE, TRANSDUCER AND ELECTRODE, PATIENT, (INCLUDING CONNECTOR) 2 SJM™
49 05414734053655 401759 401759 DSA CABLE, TRANSDUCER AND ELECTRODE, PATIENT, (INCLUDING CONNECTOR) 2 SJM™
50 05414734022149 401758 401758 DSA CABLE, TRANSDUCER AND ELECTRODE, PATIENT, (INCLUDING CONNECTOR) 2 SJM™
Other products with the same Product Code "MGB"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 M729800612C0 800-612C The VASCADE MVP Venous Vascular Closure System (VVCS) is intended to seal femora The VASCADE MVP Venous Vascular Closure System (VVCS) is intended to seal femoral veins with single or multiple access sites in one or both limbs at the completion of catheterization procedures. The system is designed to deliver a resorbable Collagen Patch, extra-vascularly, at vessel puncture sites to achieve hemostasis. For use with 6Fr to 12Fr (15F maximum outer diameter) introducer sheaths; overall length of the sheath (including the hub) needs to be less than 15cm. Cardiva VASCADE MVP VVCS 6-12F CARDIVA MEDICAL, INC.
2 M729700580I0 700-580I The VASCADE VCS is intended to seal femoral vessel puncture sites at the complet The VASCADE VCS is intended to seal femoral vessel puncture sites at the completion of catheter-based procedures. The system is designed to deliver a resorbable Collagen Patch, extra-vascularly, at the vessel puncture site to achieve hemostasis. For use in 6F & 7F introducer sheaths; overall length of the sheath (including the hub) needs to be less than 15cm. Cardiva VASCADE 6/7F VCS CARDIVA MEDICAL, INC.
3 M729700500DX0 700-500DX The VASCADE VCS is intended to seal femoral vessel puncture sites at the complet The VASCADE VCS is intended to seal femoral vessel puncture sites at the completion of catheter-based procedures. The system is designed to deliver a resorbable Collagen Patch, extra-vascularly, at the vessel puncture site to achieve hemostasis. For use in 5F introducer sheaths; overall length of the sheath (including the hub) needs to be less than 15cm. Cardiva VASCADE 5F VCS CARDIVA MEDICAL, INC.
4 10862028000434 MX6760 MX6760 Mynx Control VCD 6F 7F MYNX CONTROL ACCESS CLOSURE, INC.
5 10862028000427 MX5060 MX5060 Mynx Control VCD 5F MYNX CONTROL ACCESS CLOSURE, INC.
6 10862028000410 MX6721 MX6721 MynxGrip 6F/7F MYNXGRIP ACCESS CLOSURE, INC.
7 10862028000403 MX5021 MX5021 MynxGrip 5F MYNXGRIP ACCESS CLOSURE, INC.
8 10857141005251 202704 202704 Closer Vascular Sealing System REX MEDICAL LLP
9 10705032058896 EX700 EX700 Cordis ExoSeal Vascular Closure Device CORDIS CORPORATION
10 10705032058872 EX500 EX500 Cordis ExoSeal Vascular Closure Device CORDIS CORPORATION
11 10705032058858 EX600 EX600 Cordis ExoSeal Vascular Closure Device CORDIS CORPORATION
12 M465MX67400 MX6740 MX6740 Mynx Ace Vascular Closure Device (6F/7F) Mynx Ace Vascular Closure Device (6F/7F) ACCESS CLOSURE, INC.
13 M465MX67210 MX6721 MX6721 MynxGrip Vascular Closure Device (6F/7F) MynxGrip Vascular Closure Device (6F/7F) ACCESS CLOSURE, INC.
14 M465MX50210 MX5021 MX5021 MynxGrip Vascular Closure Device (5F) MynxGrip Vascular Closure Device (5F) ACCESS CLOSURE, INC.
15 08717648235184 12773-03 12773-03 Perclose™ ProStyle™ Suture-Mediated Closure and Repair System Perclose™ ProStyle™ ABBOTT VASCULAR INC.
16 08717648175060 14679-05 14679-05 STARCLOSE SE VCS WHITE SHEATH US STARCLOSE SE ABBOTT VASCULAR INC.
17 08717648079467 14679-01 14679-01 STARCLOSE SE Vascular Closure System STARCLOSE SE ABBOTT VASCULAR INC.
18 08717648013089 12673-03 12673-03 Perclose ProGlide™ Suture-Mediated Closure System Perclose ProGlide™ ABBOTT VASCULAR INC.
19 08717648013065 12337-04 12337-04 PERCLOSE A-T 6F Suture-Medicated Closure System PERCLOSE ABBOTT VASCULAR INC.
20 08717648000621 12322-01 12322-01 PROSTAR XL10F Percutaneous Vascular Surgical System Prostar ABBOTT VASCULAR INC.
21 05415067002877 STS Plus 610121 Angio-Seal™ ST. JUDE MEDICAL CARDIOVASCULAR DIVISION
22 05415067002860 STS Plus 610119 Angio-Seal™ ST. JUDE MEDICAL CARDIOVASCULAR DIVISION
23 05415067002853 VIP 610131 Angio-Seal™ ST. JUDE MEDICAL CARDIOVASCULAR DIVISION
24 05415067002846 Evolution™ C610135 Angio-Seal™ ST. JUDE MEDICAL CARDIOVASCULAR DIVISION
25 05415067002839 Evolution™ C610134 Angio-Seal™ ST. JUDE MEDICAL CARDIOVASCULAR DIVISION
26 05414734054591 VIP 610130 Angio-Seal™ ST. JUDE MEDICAL CARDIOVASCULAR DIVISION
27 05391530280150 KCLT-07 Celt ACD Vascular Closure Device 7F_ESP Celt ACD Vascular Closure Device 7F_ESP VASORUM LIMITED
28 05391530280129 KCLT-07 Celt ACD Vascular Closure Device 7F Celt ACD Vascular Closure Device 7F VASORUM LIMITED
29 05391530280099 KCLT-06 Celt ACD Vascular Closure Device 6F_ESP Celt ACD Vascular Closure Device 6F_ESP VASORUM LIMITED
30 05391530280068 KCLT-06 Celt ACD Vascular Closure Device 6F Celt ACD Vascular Closure Device 6F VASORUM LIMITED
31 05391530280037 KCLT-05 Celt ACD Vascular Closure Device 5F_ESP Celt ACD Vascular Closure Device 5F_ESP VASORUM LIMITED
32 04719872920380 002 002 The Cross-Seal Accessories (Cross-Seal Knot Tyer, Cross-Seal Knot Pusher, and Cr The Cross-Seal Accessories (Cross-Seal Knot Tyer, Cross-Seal Knot Pusher, and Cross-Seal Suture Trimmer) are designed to tie the knots, position the knot to the top of the arteriotomy, and to trim the trailing limbs of the suture, respectively. Cross-Seal MEDEON BIODESIGN, INC.
33 04719872920359 002 002 The Cross-Seal Device is composed of a Catheter, Suture Delivery System, and Han The Cross-Seal Device is composed of a Catheter, Suture Delivery System, and Handle.The Cross-Seal Device tracks over a standard 0.038” or 0.035” (minimum length 130 cm) guidewire. A hemostasis valve located in the middle of the CATHETER limits blood flow from the GUIDEWIRE PORT through the CATHETER with or without the guidewire in place. The SUTURE DELIVERY SYSTEM contains NEEDLES, LOCATOR WINGS, and the NEEDLE BARREL that control suture placement around the arteriotomy. The HANDLE contains the SLIDER, BLEEDING INDICATOR, PLUNGER, RESET 1 BUTTON (SLIDER RETRACTOR), and RESET 2 BUTTON (LOCATOR WINGS RETRACTOR). The SLIDER triggers a mechanism that opens the LOCATOR WINGS and creates a sandwich configuration to stabilize the delivery system within the vessel wall. The BLEEDING INDICATOR connects to a lumen that has an intraluminal port positioned at the distal end of the Suture Delivery System to allow bleeding back to ensure Suture Delivery System is positioned properly in the femoral artery. The NEEDLE BARREL keeps the Cross-Seal Device from moving deeper inside the vessel, stabilizes the device once the LOCATOR WINGS are opened and retrieves the disengaged suture-carried NEEDLES. The PLUNGER triggers the NEEDLES to deploy sutures and simultaneously close the LOCATOR WINGS. The GUIDEWIRE GUIDE is the feature at distal handle portion which allows physician to practice coaxial insertion of device along guidewire if necessary. Cross-Seal MEDEON BIODESIGN, INC.
34 00856279007246 188F MANTA 8F Depth Locator ESSENTIAL MEDICAL, INC.
35 00856279007208 114F MANTA 14F Depth Locator ESSENTIAL MEDICAL, INC.
36 00856279007079 2156 14F MANTA Vascular Closure Device MANTA ESSENTIAL MEDICAL, INC.
37 00856279007062 2115 18F MANTA Vascular Closure Device MANTA ESSENTIAL MEDICAL, INC.
38 00389701011868 610119 610119 ANGIO-SEAL STS Plus Vascular Closure Device ANGIO-SEAL TERUMO MEDICAL CORPORATION
39 00389701011851 610121 610121 ANGIO-SEAL STS Plus Vascular Closure Device ANGIO-SEAL TERUMO MEDICAL CORPORATION
40 00389701011820 610130 610130 ANGIO-SEAL VIP Vascular Closure Device ANGIO-SEAL TERUMO MEDICAL CORPORATION
41 00389701011813 610131 610131 ANGIO-SEAL VIP Vascular Closure Device ANGIO-SEAL TERUMO MEDICAL CORPORATION
42 00389701011783 C610134 C610134 ANGIO-SEAL EVOLUTION Vascular Closure Device ANGIO-SEAL TERUMO MEDICAL CORPORATION
43 00389701011776 C610135 C610135 ANGIO-SEAL EVOLUTION Vascular Closure Device ANGIO-SEAL TERUMO MEDICAL CORPORATION