No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
---|---|---|---|---|---|---|---|---|
1 | 05415067024084 | 1192 | 1192 | LGW | STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF | 3 | Swift-Lock™ | |
2 | 05414734406123 | 3183 | 3183 | LGW | STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF | 3 | Octrode™ | |
3 | 05414734202459 | 401780 | 401780 | DRF,DRA | CATHETER, ELECTRODE RECORDING, OR PROBE, ELECTRODE RECORDING,CATHETER, STEERABLE | 2 | Livewire™ | |
4 | 05414734203319 | 406805 | 406805 | DYB | INTRODUCER, CATHETER | 2 | Fast-Cath™ | |
5 | 05414734022491 | 406311 | 406311 | DYB | INTRODUCER, CATHETER | 2 | SJM™ | |
6 | 05414734011730 | 406743 | 406743 | DYB | INTRODUCER, CATHETER | 2 | Fast-Cath™ | |
7 | 05414734010832 | 406667 | 406667 | DYB | INTRODUCER, CATHETER | 2 | Maximum™ | |
8 | 05414734206938 | PL | 410187 | DQY | CATHETER, PERCUTANEOUS | 2 | CPS DIRECT™ | |
9 | 05415067017246 | 3186 | 3186 | LGW | STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF | 3 | Octrode™ | |
10 | 05415067011107 | A701124 | A701124 | OAD | catheter, percutaneous, cardiac ablation, for treatment of atrial flutter | 3 | FlexAbility™ | |
11 | 05415067025722 | X | C12359 | Guidewire | DXO,DRG,DQX | TRANSDUCER, PRESSURE, CATHETER TIP,TRANSMITTERS AND RECEIVERS, PHYSIOLOGICAL SIG TRANSDUCER, PRESSURE, CATHETER TIP,TRANSMITTERS AND RECEIVERS, PHYSIOLOGICAL SIGNAL, RADIOFREQUENCY,WIRE, GUIDE, CATHETER | PressureWire™ | |
12 | 05415067019615 | 3688 | 3688 | LGW | STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF | 3 | Eon C™ | |
13 | 05415067016560 | 3032 | 3032 | LGW | STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF | 3 | SJM™ | |
14 | 05414734506779 | DS06003/40 | DS06003/40 | DRB | STYLET, CATHETER | 2 | SJM™ | |
15 | 05414734506762 | DS06002/85 | DS06002/85 | DRB | STYLET, CATHETER | 2 | SJM™ | |
16 | 05414734505345 | DS2M028 | DS2M028 | Guidewire | DQX | WIRE, GUIDE, CATHETER | 2 | CPS Excel™ |
17 | 05414734503662 | DS06003/52 | DS06003/52 | DRB | STYLET, CATHETER | 2 | SJM™ | |
18 | 05415067018052 | H701805 | H701805 | Printer | DQK | Computer, diagnostic, programmable | 2 | NA |
19 | 05414734206914 | PL | 410185 | DQY | CATHETER, PERCUTANEOUS | 2 | CPS DIRECT™ | |
20 | 05414734406130 | 3186 | 3186 | Lead Kit, 60cm Length | LGW | STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF | 3 | Octrode™ |
21 | 05414734406024 | 3086 | 3086 | GZB | STIMULATOR, SPINAL-CORD, IMPLANTED (PAIN RELIEF) | 2 | Octrode™ | |
22 | 05414734405775 | 3852 | 3852 | Patient Programmer | LGW | STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF | 3 | NA |
23 | 05414734405133 | 1622 | 1622 | Power Adapter, RP Model 3834 | LGW | STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF | 3 | NA |
24 | 05414734403382 | 7241 | 7241 | Mobile Charger Pouch | LGW | STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF | 3 | NA |
25 | 05414734402569 | 3714 | 3714 | AC Line Cord | LGW | STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF | 3 | NA |
26 | 05414734402552 | 3713 | 3713 | AC Power Adapter | LGW | STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF | 3 | NA |
27 | 05414734402330 | 3386 | 3386 | Extension, 60cm | GZB | STIMULATOR, SPINAL-CORD, IMPLANTED (PAIN RELIEF) | 2 | NA |
28 | 05414734402323 | 3383 | 3383 | Extension, 30cm | LGW | STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF | 3 | NA |
29 | 05414734402309 | 3346 | 3346 | Extension, Dual 4 Channel 60cm | GZB | STIMULATOR, SPINAL-CORD, IMPLANTED (PAIN RELIEF) | 2 | NA |
30 | 05414734402293 | 3343 | 3343 | Extension, Dual 4 Channel 30cm | LGW | STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF | 3 | NA |
31 | 05414734402279 | 3341 | 3341 | Extension, Dual 4 Channel 10cm | LGW | STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF | 3 | NA |
32 | 05414734400206 | 1123 | 1123 | Stylet, Straight, 60cm | LGW | STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF | 3 | NA |
33 | 05414734401715 | 3189 | 3189 | Lead Kit, 90cm Length | LGW | STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF | 3 | Octrode™ |
34 | 05414734401555 | 3086 | 3086 | Trial Lead Kit, 60cm Length | GZB | STIMULATOR, SPINAL-CORD, IMPLANTED (PAIN RELIEF) | 2 | Octrode™ |
35 | 05414734401173 | 1701 | 1701 | SCS Accessory Kit Sterile | LGW | STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF | 3 | NA |
36 | 05414734400664 | 1191 | 1191 | Tunneling Tool, 0.156"¿ Diameter | HAO | INSTRUMENT, SURGICAL, NON-POWERED | 1 | NA |
37 | 05414734400657 | 1190 | 1190 | Tunneling Tool, 0.125" Diameter | HAO | INSTRUMENT, SURGICAL, NON-POWERED | 1 | NA |
38 | 05414734400237 | 1126 | 1126 | Stylet, Curved, 90cm | LGW | STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF | 3 | NA |
39 | 05414734400220 | 1125 | 1125 | Stylet, Straight, 90cm | LGW | STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF | NA | |
40 | 05414734400213 | 1124 | 1124 | Stylet, Bent, 60cm | LGW | STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF | 3 | NA |
41 | 05414734400190 | 1122 | 1122 | Stylet, Bent, 30cm | LGW | STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF | 3 | NA |
42 | 05414734400183 | 1121 | 1121 | Stylet, Straight, 30cm | LGW | STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF | 3 | NA |
43 | 05414734400145 | 1116 | 1116 | Epidural Needle, 14 gauge, 6" (15cm) | LHG,GZB | ELECTRODE, SPINAL EPIDURAL,STIMULATOR, SPINAL-CORD, IMPLANTED (PAIN RELIEF) | 2 | NA |
44 | 05414734400121 | 1114 | 1114 | Epidural Needle, 14 gauge, 4" (10cm) | GZB | STIMULATOR, SPINAL-CORD, IMPLANTED (PAIN RELIEF) | 2 | NA |
45 | 05414734400053 | 1106 | 1106 | Lead Anchor, Long | LGW | STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF | 3 | NA |
46 | 05414734400022 | 1102 | 1102 | Guide Wire for Percutaneous Leads | LGW | STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF | 3 | NA |
47 | 05414734219112 | H21911 | H21911 | Touch Screen Computer | JOQ | GENERATOR, PULSE, PACEMAKER, EXTERNAL PROGRAMMABLE | 2 | EP-4™ |
48 | 05414734206907 | PL | 410184 | DQY | CATHETER, PERCUTANEOUS | 2 | CPS DIRECT™ | |
49 | 05414734218337 | DS2A004 | DS2A004 | DQY | CATHETER, PERCUTANEOUS | 2 | CPS DIRECT™ | |
50 | 05414734218313 | SLII | DS2C017 | Slittable Outer Guide Catheter | DQY | CATHETER, PERCUTANEOUS | 2 | CPS DIRECT™ |
No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
---|---|---|---|---|---|---|
1 | 00850027837635 | 800818 | 800818 | AcQMap to DiamondTemp Generator Adapter Cable | DiamondTemp Generator Adapter | ACUTUS MEDICAL, INC. |
2 | 00850027837482 | 800748 | 800748 | Maestro Adapter Cable, AcQMap to Catheter | AcQMap | ACUTUS MEDICAL, INC. |
3 | 00850027837475 | 800745 | 800745 | Maestro Adapter Cable, AcQMap to Generator | AcQMap | ACUTUS MEDICAL, INC. |
4 | 00850027837468 | 800742 | 800742 | Adapter Cable-Long, Ablation Adapter to AcQMap | AcQMap | ACUTUS MEDICAL, INC. |
5 | 00850027837451 | 800739 | 800739 | Adapter Cable-Short, Ablation Adapter to AcQMap | AcQMap | ACUTUS MEDICAL, INC. |
6 | 00850027837444 | 800710 | 800710 | Carto Force Adapter Cable Shipping Assembly | AcQMap | ACUTUS MEDICAL, INC. |
7 | 00850027837246 | 800697 | 800697 | AcQMap to Maestro Generator Adapter | AcQMap | ACUTUS MEDICAL, INC. |
8 | 00850027837239 | 800696 | 800696 | AcQMap to SmartAblate Generator Adapter | AcQMap | ACUTUS MEDICAL, INC. |
9 | 00850027837222 | 800695 | 800695 | AcQMap to SmartAblate Generator Adapter | AcQMap | ACUTUS MEDICAL, INC. |
10 | 00850027837192 | 800698 | 800698 | SmartAblate™ Adapter Cable AcQMap to Catheter | AcQMap | ACUTUS MEDICAL, INC. |
11 | 00850022994173 | Merge 3.5mm, Type I | 512-134 | Zurich Medical Accessory Cable | ZURICH MEDICAL INC. | |
12 | 00850022994166 | Merge 3.5mm, Type G | 512-133 | Zurich Medical Accessory Cable | ZURICH MEDICAL INC. | |
13 | 00850022994159 | Merge 3.5mm, Type C | 512-132 | Zurich Medical Accessory Cable | ZURICH MEDICAL INC. | |
14 | 00850022994142 | Merge 3.5mm, Type A | 512-131 | Zurich Medical Accessory Cable | ZURICH MEDICAL INC. | |
15 | 00850022994128 | GE 9-Pin, Type I | 512-024 | Zurich Medical Accessory Cable | ZURICH MEDICAL INC. | |
16 | 00850022994111 | GE 9-Pin, Type G | 512-023 | Zurich Medical Accessory Cable | ZURICH MEDICAL INC. | |
17 | 00850022994104 | GE 9-Pin, Type C | 512-022 | Zurich Medical Accessory Cable | ZURICH MEDICAL INC. | |
18 | 00850022994098 | GE 9-Pin, Type A | 512-021 | Zurich Medical Accessory Cable | ZURICH MEDICAL INC. | |
19 | 00850022994081 | Philips BNC, Type I | 512-124 | Zurich Medical Accessory Cable | ZURICH MEDICAL INC. | |
20 | 00850022994074 | Philips BNC, Type G | 512-123 | Zurich Medical Accessory Cable | ZURICH MEDICAL INC. | |
21 | 00850022994067 | Philips BNC, Type C | 512-122 | Zurich Medical Accessory Cable | ZURICH MEDICAL INC. | |
22 | 00850022994050 | Philips BNC, Type A | 512-121 | Zurich Medical Accessory Cable | ZURICH MEDICAL INC. | |
23 | 00850022994043 | GE 7-Pin, Type I | 512-004 | Zurich Medical Accessory Cable | ZURICH MEDICAL INC. | |
24 | 00850022994036 | GE 7-Pin, Type G | 512-003 | Zurich Medical Accessory Cable | ZURICH MEDICAL INC. | |
25 | 00850022994029 | GE-7-Pin, Type C | 512-002 | Zurich Medical Accessory Cable | ZURICH MEDICAL INC. | |
26 | 00850022994012 | GE-7-Pin, Type A | 512-001 | Zurich Medical Accessory Cable | ZURICH MEDICAL INC. | |
27 | 00850022994005 | Model 100 | 308 | Zurich Pressure Guidewire System | ZURICH MEDICAL INC. | |
28 | 00843152104000 | SW-1 | SW-1 | The IOPS (Intra-Operative Positioning System) is intended for the evaluation of The IOPS (Intra-Operative Positioning System) is intended for the evaluation of vascular anatomy as captured using 3D modeling from previously acquired scan data. It is intended for real-time tip positioning and navigation using sensor-equipped, compatible catheters and guidewires used in endovascular interventions in the descending aorta. After the patient is placed on the OR table, a cone beam CT (CBCT) is acquired using fluoroscopy with a flat panel detector (FPD). The scan is uploaded to the hospital’s PACS. The CBCT is registered to the initial CT using the IOPS software and the 3D renderings. The system is indicated for use as an adjunct to fluoroscopy. The IOPS does not make a diagnosis. | IOPS™ Software Application | CENTERLINE BIOMEDICAL, INC. |
29 | 00843152103003 | TP-1 | TP-1 | IOPS™ Tracking Pad 1 | IOPS™ | CENTERLINE BIOMEDICAL, INC. |
30 | 00843152102037 | ATW-2 | ATW-2 | IOPS™ Guidewire 2 | IOPS™ | CENTERLINE BIOMEDICAL, INC. |
31 | 00843152102013 | SSH-1 | SSH-1 | IOPS™ Guidewire 2 Handle for connection of guidewire sensor to system | IOPS™ | CENTERLINE BIOMEDICAL, INC. |
32 | 00843152101030 | RCC-1 | RCC-1 | IOPS™ Catheter Reverse Curve 1 | IOPS™ | CENTERLINE BIOMEDICAL, INC. |
33 | 00843152101023 | SCC-1 | SCC-1 | IOPS™ Catheter Simple Curve 1 | IOPS™ | CENTERLINE BIOMEDICAL, INC. |
34 | 00843152100002 | MC-1 | MC-1 | The IOPS (Intra-Operative Positioning System) is intended for the evaluation of The IOPS (Intra-Operative Positioning System) is intended for the evaluation of vascular anatomy as captured using 3D modeling from previously acquired scan data. It is intended for real-time tip positioning and navigation using sensor-equipped, compatible catheters and guidewires used in endovascular interventions in the descending aorta. After the patient is placed on the OR table, a cone beam CT (CBCT) is acquired using fluoroscopy with a flat panel detector (FPD). The scan is uploaded to the hospital’s PACS. The CBCT is registered to the initial CT using the IOPS software and the 3D renderings. The system is indicated for use as an adjunct to fluoroscopy. The IOPS does not make a diagnosis. | IOPS Mobile Cart | CENTERLINE BIOMEDICAL, INC. |
35 | 00842000100966 | 10.4 | Merge Hemo | MERGE HEALTHCARE SOLUTIONS INC. | ||
36 | 00842000100874 | 10.3 | Merge Hemo | MERGE HEALTHCARE SOLUTIONS INC. | ||
37 | 00842000100515 | 77-00327-00 | Merge Hemo 77-00327-00 Link Assembly | Merge Hemo Link Assembly | MERGE HEALTHCARE SOLUTIONS INC. | |
38 | 00842000100447 | 11.0 | Correcting entry. | Merge Hemo | MERGE HEALTHCARE SOLUTIONS INC. | |
39 | 00842000100430 | 10.2 | Merge Hemo | MERGE HEALTHCARE SOLUTIONS INC. | ||
40 | 00842000100034 | 10.1 | Merge HEMO | MERGE HEALTHCARE SOLUTIONS INC. | ||
41 | 00842000100027 | 9.4 | Merge Hemo | MERGE HEALTHCARE SOLUTIONS INC. | ||
42 | 00842000100010 | 10.0.4 | Merge Hemo | MERGE HEALTHCARE SOLUTIONS INC. | ||
43 | 00841268100541 | SGW-011-08 | SGW-011-08 | Guidewire | Guidewire | GALT MEDICAL CORP. |
44 | 00840682188968 | BT21 | MLCL Upgrade | GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES, INC. | ||
45 | 00840682152754 | NotifyMe V1.0 | MD ACUTE VIRTUAL COLLABORATOR NOTIFY ME 1.0 | Graffiti | GE HEALTHCARE | |
46 | 00840682147224 | B125P VSP3.0 Patient Monitor | 6160000-002 | B125P ATO MODEL | NA | GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES, INC. |
47 | 00840682147217 | B105P VSP3.0 Patient Monitor | 6160000-001 | B105P ATO MODEL | NA | GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES, INC. |
48 | 00840682146791 | B155 VSP3.0 Patient Monitor | 6160000-005 | B155M ATO MODEL | NA | GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES, INC. |
49 | 00840682146715 | B125 VSP3.0 Patient Monitor | 6160000-004 | B125M ATO MODEL | NA | GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES, INC. |
50 | 00840682146708 | B105 VSP3.0 Patient Monitor | 6160000-003 | B105M ATO MODEL | NA | GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES, INC. |