Other products from "MEDTRONIC, INC."
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 00763000500993 BB11N31R1 CUSTOM PACK BB11N31R1 RESEARCH PACK DWF Catheter, cannula and tubing, vascular, cardiopulmonary bypass 2 NA
2 00763000500979 BB11N23R CUSTOM PACK BB11N23R 10PK XTRASUC DWF Catheter, cannula and tubing, vascular, cardiopulmonary bypass 2 NA
3 00763000500962 BB10R11R5 CUSTOM PACK BB10R11R5 PUMP PK DWF Catheter, cannula and tubing, vascular, cardiopulmonary bypass 2 NA
4 00763000500948 BB5Z34R5 CUSTOM PACK BB5Z34R5 NURSES DWF Catheter, cannula and tubing, vascular, cardiopulmonary bypass 2 NA
5 00763000500931 BB11G46R1 CUSTOM PACK BB11G46R1 RQST2 DWF Catheter, cannula and tubing, vascular, cardiopulmonary bypass 2 NA
6 00763000500634 7H97R2 CUSTOM PACK 7H97R2 25PK FEMALE ADAPT DWF Catheter, cannula and tubing, vascular, cardiopulmonary bypass 2 NA
7 00763000500559 HY10Z01R8 CUSTOM PACK HY10Z01R8 SUPPORT PACK DWF Catheter, cannula and tubing, vascular, cardiopulmonary bypass 2 NA
8 00763000501105 BB5B82R2 CUSTOM PACK BB5B82R2 5PK SUPPLE 2 DWF Catheter, cannula and tubing, vascular, cardiopulmonary bypass 2 NA
9 00763000511555 ONYXNG35012UX STENT ONYXNG35012UX ONYX 3.50X12RX NIQ Coronary drug-eluting stent 3 Onyx Frontier™
10 00763000498535 BB11L44R2 CUSTOM PACK BB11L44R2 OPEN HEART DWF Catheter, cannula and tubing, vascular, cardiopulmonary bypass 2 NA
11 00763000511470 ONYXNG30015UX STENT ONYXNG30015UX ONYX 3.00X15RX NIQ Coronary drug-eluting stent 3 Onyx Frontier™
12 00763000511418 ONYXNG27526UX STENT ONYXNG27526UX ONYX 2.75X26RX NIQ Coronary drug-eluting stent 3 Onyx Frontier™
13 00763000511326 ONYXNG25026UX STENT ONYXNG25026UX ONYX 2.50X26RX NIQ Coronary drug-eluting stent 3 Onyx Frontier™
14 00763000489472 HY7Y30R18 CUSTOM PACK HY7Y30R18 EC AMBU DWF Catheter, cannula and tubing, vascular, cardiopulmonary bypass 2 NA
15 00763000489434 BB7L75R3 CUSTOM PACK BB7L75R3 10PK 3/8X 72 DWF Catheter, cannula and tubing, vascular, cardiopulmonary bypass 2 NA
16 00763000426422 B3301533M LEAD B3301533M SENSIGHT 1.5MM EMAN LJ53 MHY,MRU,NHL,PJS,MBX Stimulator, electrical, implanted, for parkinsonian tremor,implanted subcortical Stimulator, electrical, implanted, for parkinsonian tremor,implanted subcortical electrical Stimulator (motor disorders),Stimulator, electrical, implanted, for parkinsonian symptoms,Stimulator, electrical, implanted, for essential tremor,Stimulator, thalamic, epilepsy, implanted 3 SenSight™
17 00763000426408 B3300542M LEAD B3300542M SENSIGHT 0.5MM EMAN LJ53 MBX,NHL,MRU,PJS,MHY Stimulator, thalamic, epilepsy, implanted,Stimulator, electrical, implanted, for Stimulator, thalamic, epilepsy, implanted,Stimulator, electrical, implanted, for parkinsonian symptoms,implanted subcortical electrical Stimulator (motor disorders),Stimulator, electrical, implanted, for essential tremor,Stimulator, electrical, implanted, for parkinsonian tremor 3 SenSight™
18 00763000334178 11D35R CUSTOM PACK 11D35R RETO5 DWF Catheter, cannula and tubing, vascular, cardiopulmonary bypass 2 NA
19 00763000334130 11D33R CUSTOM PACK 11D33R RETO1 DWF Catheter, cannula and tubing, vascular, cardiopulmonary bypass 2 NA
20 00763000306144 ETBF3216C166E STENT GRAFT ETBF3216C166E ENDUR II BIF MIH SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT 3 Endurant® II
21 00763000305659 ETLW1624C93E STENT GRAFT ETLW1624C93E ENDUR II LIMB MIH SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT 3 Endurant® II
22 00763000305598 ETLW1620C82E STENT GRAFT ETLW1620C82E ENDUR II LIMB MIH SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT 3 Endurant® II
23 00763000271220 7800RR36 RING 7800RR36 SIMUFORM SR 36MM US KRH RING, ANNULOPLASTY 2 SimuForm™
24 00763000271107 7700FR32 RING 7700FR32 SIMUPLUS FLEX 32MM US KRH RING, ANNULOPLASTY 2 SimuPlus™
25 00763000499945 BB5U74R18 CUSTOM PACK BB5U74R18 TUBING DWF Catheter, cannula and tubing, vascular, cardiopulmonary bypass 2 NA
26 00763000499921 BB8S37R29 CUSTOM PACK BB8S37R29 PUMP TBL DWF Catheter, cannula and tubing, vascular, cardiopulmonary bypass 2 NA
27 00763000511647 ONYXNG40012UX STENT ONYXNG40012UX ONYX 4.00X12RX NIQ Coronary drug-eluting stent 3 Onyx Frontier™
28 00763000498870 CB11N89R CUSTOM PACK CB11N89R MAN/BRIDGE DWF Catheter, cannula and tubing, vascular, cardiopulmonary bypass 2 NA
29 00763000260743 VNMC2828C90TU STENT GRAFT VNMC2828C90TU VAL NAV CS MIH SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT 3 Valiant Navion™
30 00763000001377 BB8B73R7 CUSTOM PACK BB8B73R7 PK DWE TUBING, PUMP, CARDIOPULMONARY BYPASS 2 NA
31 00681490024273 05328 CABLE 05328 ATAKR EGM SAFETY 8FT LPB Cardiac ablation percutaneous catheter 3 NA
32 00673978549071 5344 PLUG 5344 1/4 INCH DWE TUBING, PUMP, CARDIOPULMONARY BYPASS 2 NA
33 00643169796454 AB9U20100090 STENT AB9U20100090 ABRE V01 QAN Stent, iliac vein 3 Abre™
34 00643169518919 97740 PROG 97740 PATIENT MRICS SCS USA ROHS LGW STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF 3 NA
35 00643169078024 500FA27 MHV 500FA27 STD AORTIC LWQ HEART-VALVE, MECHANICAL 3 Open Pivot™
36 00613994759221 680R32 RING 680R32 PROFILE 3D 26L MEXICO KRH RING, ANNULOPLASTY 2 PROFILE 3D®
37 00613994691392 37642 PRGMR 37642 PATIENT DBS W SC,PC,RC MFR,NHL,MHY,OLM,MRU Stimulator, brain, implanted, for behavior modification,STIMULATOR, ELECTRICAL, Stimulator, brain, implanted, for behavior modification,STIMULATOR, ELECTRICAL, IMPLANTED, FOR PARKINSONIAN SYMPTOMS,STIMULATOR, ELECTRICAL, IMPLANTED, FOR PARKINSONIAN TREMOR,Deep brain stimulator for obsessive compulsive disorder (OCD),implanted subcortical electrical Stimulator (motor disorders) 3 NA
38 00613994334565 68005YN CABLE 68005YN EGM 18L OCL Surgical Device, For cutting, coagulation, and/or ablation of tissue, including Surgical Device, For cutting, coagulation, and/or ablation of tissue, including cardiac tissue 2 NA
39 00885074469669 365538 TUNNEL TOOL 365538 ACCESSORY KIT US MKT HAO INSTRUMENT, SURGICAL, NON-POWERED 1 NA
40 00885074375458 SB7MAC30 CATHETER SB7MAC30 SB 7F 100CM MA30 DQY CATHETER, PERCUTANEOUS 2 SHERPA NX BALANCED
41 00885074372181 SB7EBU40D CATHETER SB7EBU40D SB 7F 90CM EB40 DQY CATHETER, PERCUTANEOUS 2 SHERPA NX BALANCED
42 00763000665982 BB11V67R3 CUSTOM PACK BB11V67R3 UMC DWF Catheter, cannula and tubing, vascular, cardiopulmonary bypass 2 NA
43 00763000552985 CB11J56R3 CUSTOM PACK CB11J56R3 PEDI MAG DWF Catheter, cannula and tubing, vascular, cardiopulmonary bypass 2 NA
44 00763000541118 6A32R2 CUSTOM PACK 6A32R2 1/4X1/4 DWF Catheter, cannula and tubing, vascular, cardiopulmonary bypass 2 NA
45 00763000400866 3320L LIT 3320L DYSTONIA EMANUALS EN MRU implanted subcortical electrical Stimulator (motor disorders) N/A
46 00763000502843 FMET-IM-SYS-S SYSTEM SERVICED FMET-IM-SYS-S DPW FLOWMETER, BLOOD, CARDIOVASCULAR 2 FlowMet™
47 00763000390891 LA6ERADRST CATHETER LA6ERADRST LA 6F 100CM ERDRS DQY Catheter, percutaneous 2 Launcher
48 00763000310332 37601 INS 37601 ACTIVA PC DBS EMANUAL EN OLM,MRU,MHY,NHL,MBX,PJS Deep brain stimulator for obsessive compulsive disorder (OCD),implanted subcorti Deep brain stimulator for obsessive compulsive disorder (OCD),implanted subcortical electrical Stimulator (motor disorders),STIMULATOR, ELECTRICAL, IMPLANTED, FOR PARKINSONIAN TREMOR,Stimulator, electrical, implanted, for parkinsonian symptoms,STIMULATOR, THALAMIC, EPILEPSY, IMPLANTED,Stimulator, electrical, implanted, for essential tremor 3 Activa® PC
49 00763000306519 104FS FOOTSWITCH 104FS CRYOCONSOLE MDR LPB Cardiac ablation percutaneous catheter 3 N/A
50 00763000301330 HC150A HANDCRANK HC150A PLX 31L DWA Control, pump speed, cardiopulmonary bypass 2 Affinity™
Other products with the same Product Code "JWH"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 28031497001900 SPK0722 Temporary Augmented Tibial Stem Spacer with gentamicin. Interspace Knee ATS is c Temporary Augmented Tibial Stem Spacer with gentamicin. Interspace Knee ATS is composed of fully formed gentamicin/polymethylmethacrylate (PMMA), radio-opaque bone cement. The device is sterile and single-use.InterSpace Knee ATS is indicated for temporary use (maximum 180 days) as an adjunct to total knee replacement (TKR) in skeletally mature patients undergoing a two-stage procedure due to a septic process, and where a large tibial defect is present.InterSpace Knee ATS is applied on the tibial plate following removal of the existing implant and radical debridement. The device must be combined with the tibial component of InterSpace Knee. The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy (standard treatment approach to an infection).InterSpace Knee ATS is not intended for use for more than 180 days, at which time it must be explanted and a permanent device implanted or another appropriate treatment performed (e.g. resection arthroplasty, fusion etc.). Because of the inherent mechanical limitations of the device material (gentamicin/ polymethylmethacrylate), the Interspace Knee ATS is only indicated for patients who will consistently use traditional mobility assist devices (e.g. crutches, walkers, canes) throughout the implantation period. Interspace Knee ATS 80/12 TECRES SPA
2 28031497001894 SPK0622 Temporary Augmented Tibial Stem Spacer with gentamicin. Interspace Knee ATS is c Temporary Augmented Tibial Stem Spacer with gentamicin. Interspace Knee ATS is composed of fully formed gentamicin/polymethylmethacrylate (PMMA), radio-opaque bone cement. The device is sterile and single-use.InterSpace Knee ATS is indicated for temporary use (maximum 180 days) as an adjunct to total knee replacement (TKR) in skeletally mature patients undergoing a two-stage procedure due to a septic process, and where a large tibial defect is present.InterSpace Knee ATS is applied on the tibial plate following removal of the existing implant and radical debridement. The device must be combined with the tibial component of InterSpace Knee. The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy (standard treatment approach to an infection).InterSpace Knee ATS is not intended for use for more than 180 days, at which time it must be explanted and a permanent device implanted or another appropriate treatment performed (e.g. resection arthroplasty, fusion etc.). Because of the inherent mechanical limitations of the device material (gentamicin/ polymethylmethacrylate), the Interspace Knee ATS is only indicated for patients who will consistently use traditional mobility assist devices (e.g. crutches, walkers, canes) throughout the implantation period. Interspace Knee ATS 80/07 TECRES SPA
3 28031497001887 SPK0522 Temporary Augmented Tibial Stem Spacer with gentamicin. Interspace Knee ATS is c Temporary Augmented Tibial Stem Spacer with gentamicin. Interspace Knee ATS is composed of fully formed gentamicin/polymethylmethacrylate (PMMA), radio-opaque bone cement.The device is sterile and single-use.InterSpace Knee ATS is indicated for temporary use (maximum 180 days) as an adjunct to total knee replacement (TKR) in skeletally mature patients undergoing a two-stage procedure due to a septic process, and where a large tibial defect is present.InterSpace Knee ATS is applied on the tibial plate following removal of the existing implant and radical debridement. The device must be combined with the tibial component of InterSpace Knee. The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy (standard treatment approach to an infection).InterSpace Knee ATS is not intended for use for more than 180 days, at which time it must be explanted and a permanent device implanted or another appropriate treatment performed (e.g. resection arthroplasty, fusion etc.). Because of the inherent mechanical limitations of the device material (gentamicin/ polymethylmethacrylate), the Interspace Knee ATS is only indicated for patients who will consistently use traditional mobility assist devices (e.g. crutches, walkers, canes) throughout the implantation period. Interspace Knee ATS 60/12 TECRES SPA
4 28031497001870 SPK0422 Temporary Augmented Tibial Stem Spacer with gentamicin. Interspace Knee ATS is c Temporary Augmented Tibial Stem Spacer with gentamicin. Interspace Knee ATS is composed of fully formed gentamicin/polymethylmethacrylate (PMMA), radio-opaque bone cement. The device is sterile and single-use.InterSpace Knee ATS is indicated for temporary use (maximum 180 days) as an adjunct to total knee replacement (TKR) in skeletally mature patients undergoing a two-stage procedure due to a septic process, and where a large tibial defect is present.InterSpace Knee ATS is applied on the tibial plate following removal of the existing implant and radical debridement. The device must be combined with the tibial component of InterSpace Knee. The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy (standard treatment approach to an infection).InterSpace Knee ATS is not intended for use for more than 180 days, at which time it must be explanted and a permanent device implanted or another appropriate treatment performed (e.g. resection arthroplasty, fusion etc.). Because of the inherent mechanical limitations of the device material (gentamicin/ polymethylmethacrylate), the Interspace Knee ATS is only indicated for patients who will consistently use traditional mobility assist devices (e.g. crutches, walkers, canes) throughout the implantation period. Interspace Knee ATS 60/07 TECRES SPA
5 28031497001160 SPK0322 Temporary knee spacer with gentamicin. InterSpace Knee is composed of fully form Temporary knee spacer with gentamicin. InterSpace Knee is composed of fully formed gentamicin/polymethylmethacrylate (PMMA) radiopaque bone cement.The device is sterile and single-use.InterSpace Knee is indicated for temporary use (maximum 180 days) as a total knee replacement (TKR) in skeletally mature patients undergoing a two-stage procedure due to a septic process.InterSpace Knee is applied on the femoral condyles and on the tibial plate following removal of the existing implant and radical debridement. The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy (standard treatment approach to an infection).InterSpace Knee is not intended for use for more than 180 days, at which time it must be explanted and a permanent device implanted or another appropriate treatment performed (e.g. resection arthroplasty, fusion etc.). Because of the inherent mechanical limitations of the device material (gentamicin/polymethylmethacrylate), Interspace Knee is only indicated for patients who will consistently use traditional mobility assist devices (e.g. crutches, walkers, canes) throughout the implantation period. InterSpace Knee TECRES SPA
6 28031497000606 SPK0222 Temporary knee spacer with gentamicin. InterSpace Knee is composed of fully form Temporary knee spacer with gentamicin. InterSpace Knee is composed of fully formed gentamicin/polymethylmethacrylate (PMMA) radiopaque bone cement.The device is sterile and single-use.InterSpace Knee is indicated for temporary use (maximum of 180 days) as a total knee replacement (TKR) in skeletally mature patients undergoing a two-stage procedure due to a septic process. InterSpace Knee is applied on the femoral condyles and on the tibial plate following removal of the existing implantand radical debridement. The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy (standard treatment approach to an infection). InterSpace Knee is not intended for use for more than 180 days, at which time it must be explanted and a permanent device implanted or another appropriate treatment performed (e.g., resection arthroplasty, fusion, etc.). InterSpace Knee TECRES SPA
7 28031497000590 SPK0122 Temporary knee spacer with gentamicin. InterSpace Knee is composed of fully form Temporary knee spacer with gentamicin. InterSpace Knee is composed of fully formed gentamicin/polymethylmethacrylate (PMMA) radiopaque bone cement.The device is sterile and single-use.InterSpace Knee is indicated for temporary use (maximum of 180 days) as a total knee replacement (TKR) in skeletally mature patients undergoing a two-stage procedure due to a septic process. InterSpace Knee is applied on the femoral condyles and on the tibial plate following removal of the existing implantand radical debridement. The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy (standard treatment approach to an infection). InterSpace Knee is not intended for use for more than 180 days, at which time it must be explanted and a permanent device implanted or another appropriate treatment performed (e.g., resection arthroplasty, fusion, etc.). InterSpace Knee TECRES SPA
8 28031497000583 SPK0022 Temporary knee spacer with gentamicin. InterSpace Knee is composed of fully form Temporary knee spacer with gentamicin. InterSpace Knee is composed of fully formed gentamicin/polymethylmethacrylate (PMMA) radiopaque bone cement.The device is sterile and single-use.InterSpace Knee is indicated for temporary use (maximum of 180 days) as a total knee replacement (TKR) in skeletally mature patients undergoing a two-stage procedure due to a septic process. InterSpace Knee is applied on the femoral condyles and on the tibial plate following removal of the existing implantand radical debridement. The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy (standard treatment approach to an infection). InterSpace Knee is not intended for use for more than 180 days, at which time it must be explanted and a permanent device implanted or another appropriate treatment performed (e.g., resection arthroplasty, fusion, etc.). InterSpace Knee TECRES SPA
9 10885862621931 SPI-046699 SPI-046699 Special Pinned Femoral RT- INT/ LT-EXT Rotation Adjustment Block Truliant EXACTECH, INC.
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28 10885862606853 SPI-041550-3 SPI-041550-3 Truliant EXACTECH, INC.
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