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™ |
No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
---|---|---|---|---|---|---|
1 | B55880004421 | 800-0442 | 800-0442 | The aiACT Kit is an in vitro diagnostic test for use with the Sonoclot® Coagulat The aiACT Kit is an in vitro diagnostic test for use with the Sonoclot® Coagulation & Platelet Function Analyzer System. The aiACT test is an activated whole blood clotting time test which uses a blend of celite and clay for contact activation. It may also be used with citrated whole blood.The aiACT Kit is only intended for high dose (ACT greater or equal to 400 seconds, on Sonoclot Analyzer) heparin anticoagulation management as typically encountered during cardiopulmonary bypass surgery. The aiACT test provides ACT results that are substantially unaffected by aprotinin. When used with the Sonoclot Analyzer System, the aiACT test provides quantitative Onset/ACT and Clot Rate results. Do not use the aiACT test for platelet function assessment. Each kit contains 100 lidded yellow plastic activation cuvettes, 100 probes, and instructions for use. The activation cuvettes contain a controlled amount of contact activator and a magnetic stir bar. | Sonoclot® aiACT Kit | SIENCO, INC. |
2 | B55880004411 | 800-0441 | 800-0441 | The aiACT Kit is an in vitro diagnostic test for use with the Sonoclot® Coagulat The aiACT Kit is an in vitro diagnostic test for use with the Sonoclot® Coagulation & Platelet Function Analyzer System. The aiACT test is an activated whole blood clotting time test which uses a blend of celite and clay for contact activation. It may also be used with citrated whole blood.The aiACT Kit is only intended for high dose (ACT greater or equal to 400 seconds, on Sonoclot Analyzer) heparin anticoagulation management as typically encountered during cardiopulmonary bypass surgery. The aiACT test provides ACT results that are substantially unaffected by aprotinin. When used with the Sonoclot Analyzer System, the aiACT test provides quantitative Onset/ACT and Clot Rate results. Do not use the aiACT test for platelet function assessment. Each kit contains 24 lidded yellow plastic activation cuvettes, 24 probes, and instructions for use. The activation cuvettes contain a controlled amount of contact activator and a magnetic stir bar. | Sonoclot® aiACT Kit | SIENCO, INC. |
3 | B55880004121 | 800-0412 | 800-0412 | The gbACT+ Kit is an in vitro diagnostic reagent for use with the Sonoclot® Coag The gbACT+ Kit is an in vitro diagnostic reagent for use with the Sonoclot® Coagulation & Platelet Function Analyzer System. The gbACT+ test is a glass bead activated whole blood clotting time test. It may also be used with citrated whole blood and plasma. Warning: The gbACT+ test is not intended for high dose heparin management during cardiopulmonary bypass surgery.The gbACT+ Kit is intended for general purpose global hemostasis monitoring including: clot detection, fibrin formation, platelet function, and hyperfibrinolysis. The monitoring information is typically used for anticoagulant management at low to moderate heparin levels (0 to 2 units per ml), hypercoagulable and/or hypocoagulable screening, platelet function assessment, and hyperfibrinolysis screening.When used with the Sonoclot Analyzer System, the gbACT+ test provides quantitative Onset/ACT and Clot Rate results as well as qualitative and quantitative information on the Sonoclot Signature including: fibrin formation, platelet function, and hyperfibrinolysis.Each kit contains 100 lidded pink plastic activation cuvettes, 100 probes, and instructions for use. The activation cuvettes contain a controlled amount of glass beads and a magnetic stir bar. | Sonoclot® gbACT+ Kit | SIENCO, INC. |
4 | B55880004111 | 800-0411 | 800-0411 | The gbACT+ Kit is an in vitro diagnostic reagent for use with the Sonoclot® Coag The gbACT+ Kit is an in vitro diagnostic reagent for use with the Sonoclot® Coagulation & Platelet Function Analyzer System. The gbACT+ test is a glass bead activated whole blood clotting time test. It may also be used with citrated whole blood and plasma. Warning: The gbACT+ test is not intended for high dose heparin management during cardiopulmonary bypass surgery.The gbACT+ Kit is intended for general purpose global hemostasis monitoring including: clot detection, fibrin formation, platelet function, and hyperfibrinolysis. The monitoring information is typically used for anticoagulant management at low to moderate heparin levels (0 to 2 units per ml), hypercoagulable and/or hypocoagulable screening, platelet function assessment, and hyperfibrinolysis screening.When used with the Sonoclot Analyzer System, the gbACT+ test provides quantitative Onset/ACT and Clot Rate results as well as qualitative and quantitative information on the Sonoclot Signature including: fibrin formation, platelet function, and hyperfibrinolysis.Each kit contains 24 lidded pink plastic activation cuvettes, 24 probes, and instructions for use. The activation cuvettes contain a controlled amount of glass beads and a magnetic stir bar. | Sonoclot® gbACT+ Kit | SIENCO, INC. |
5 | 20812747018088 | 07-032 | RAPIDTEG REAGENT | TEG5000 HEMOSTASIS SYSTEM | HAEMONETICS CORPORATION | |
6 | 20763000014869 | 550-12 | CONTROL 550-12 CLOTTRAC HTC 15BX | CLOTtrac™ | MEDTRONIC, INC. | |
7 | 20763000014852 | 550-10 | CONT 550-10 CLOTTRAC RACT ABN 11L 15BX | CLOTtrac™ | MEDTRONIC, INC. | |
8 | 20763000014845 | 550-09 | CONT 550-09 CLOTTRAC LR ABN BXD ASY 15BX | CLOTtrac™ | MEDTRONIC, INC. | |
9 | 20763000014838 | 550-08 | CONT 550-08 CLOTTRAC HR ABN BXD ASY 15BX | CLOTtrac™ | MEDTRONIC, INC. | |
10 | 20763000014821 | 550-07 | CONTROL 550-07 CLOTTRAC HR 11L 15BX | CLOTtrac™ | MEDTRONIC, INC. | |
11 | 20643169730155 | 304-20POR | CRTG 304-20POR PORC HDR 5L INT 9BX | N/A | MEDTRONIC, INC. | |
12 | 20643169713264 | 402-07 | CARTRIDGE 402-07 HR HTC BXD 11L 20BX | NA | MEDTRONIC, INC. | |
13 | 20643169577491 | 402-03 | CARTRIDGE 402-03 ACT HR 13 LAN | HR-ACT | MEDTRONIC, INC. | |
14 | 20643169577460 | 402-01 | CARTRIDGE 402-01 ACT LR 13 LAN | LR-ACT | MEDTRONIC, INC. | |
15 | 20613994923343 | 550-12 | BOXED 550-12 CLOTTRAC HTC CONTROL | CLOTtrac® | MEDTRONIC, INC. | |
16 | 20613994923275 | 304-20POR | CRTG 304-20POR PORC HDR 5L INT 9BX | NA | MEDTRONIC, INC. | |
17 | 20613994417293 | 402-03 | CARTRIDGE 402-03 ACT HR 13 LAN | HR-ACT | MEDTRONIC, INC. | |
18 | 10885074184927 | 550-10 | CONT 550-10 CLOTTRAC RACT ABN 11L 15BX | CLOTtrac® | MEDTRONIC, INC. | |
19 | 10885074184910 | 550-09 | CONT 550-09 CLOTTRAC LR ABN BXD ASY 15BX | CLOTtrac® | MEDTRONIC, INC. | |
20 | 10885074184880 | 550-08 | CONT 550-08 CLOTTRAC HR ABN BXD ASY 15BX | CLOTtrac® | MEDTRONIC, INC. | |
21 | 10885074184873 | 550-07 | CONTROL 550-07 CLOTTRAC HR 11L 15BX | CLOTtrac® | MEDTRONIC, INC. | |
22 | 10885074117314 | 402-07 | CARTRIDGE 402-07 HR HTC BXD 11L 20BX | HR HTC | MEDTRONIC, INC. | |
23 | 10711234103418 | 000GACT-LR | 000GACT-LR | GH100 ACT-LR 45 cuvettes/box | GEM Hemochron 100 Low Range Activated Clotting Time Test (ACT-LR) | ACCRIVA DIAGNOSTICS HOLDINGS, INC. |
24 | 10711234103401 | 000GACT+ | 000GACT+ | GH100 ACT+ 45 cuvettes/box. | GEM Hemochron 100 Activated Clotting Time Plus Test (ACT+) | ACCRIVA DIAGNOSTICS HOLDINGS, INC. |
25 | 10711234103081 | JACT-LR | JACT-LR | ACT-Low Range Cuvettes - 45 cuvettes/box. | Hemochron Whole Blood Microcoagulation System | ACCRIVA DIAGNOSTICS HOLDINGS, INC. |
26 | 10711234103067 | JACT+ | JACT+ | ACT+ Cuvette - 45 cuvettes/box. | Hemochron Whole Blood Microcoagulation System | ACCRIVA DIAGNOSTICS HOLDINGS, INC. |
27 | 10711234101391 | HRFTK-ACT | HRFTK-ACT | Kaolin ACT Tubes - 95 tubes/box | Hemochron Whole Blood Coagulation System | ACCRIVA DIAGNOSTICS HOLDINGS, INC. |
28 | 10711234101384 | HRFTCA510 | HRFTCA510 | Celite ACT Tubes - 95 tubes/box | Hemochron Whole Blood Coagulation System | ACCRIVA DIAGNOSTICS HOLDINGS, INC. |
29 | 10711234101094 | P214 | P214 | ACT Tubes 95 tubes/box | Hemochron Whole Blood Coagulation System | ACCRIVA DIAGNOSTICS HOLDINGS, INC. |
30 | M525MAXACT0 | MAX-ACT | Actalyke MAX-ACT Tubes | HELENA LABORATORIES CORPORATION | ||
31 | M525KACT0 | K-ACT | K-ACT Tubes | HELENA LABORATORIES CORPORATION | ||
32 | M525GACT0 | G-ACT | G-ACT Tubes | HELENA LABORATORIES CORPORATION | ||
33 | M525CACT0 | C-ACT | C-ACT Tubes | HELENA LABORATORIES CORPORATION | ||
34 | M52557700040 | 5770004 | Actalyke XL, (CSA/CE), W/ Flash Memory | HELENA LABORATORIES CORPORATION | ||
35 | M52557700030 | 5770003 | Actalyke XL, (CSA/CE), New Display #2 (110V/220V) | HELENA LABORATORIES CORPORATION | ||
36 | M52557700020 | 5770002 | Actalyke XL, Dual Detection, (Display #2) "CE" (110V/220V) | HELENA LABORATORIES CORPORATION | ||
37 | M52557700010 | 5770001 | Actalyke XL, Dual Detection, (New Display) "CE" (110V/220V) | HELENA LABORATORIES CORPORATION | ||
38 | M52557550010 | 5755001 | Actalyke Mini II, w/o Printer & Battery, "CE 2009" (110V/220V) | HELENA LABORATORIES CORPORATION | ||
39 | M52557550000 | 5755000 | Actalyke Mini II, w/o Printer & Battery., "CE" (110V/220V) | HELENA LABORATORIES CORPORATION | ||
40 | M52557530010 | 5753001 | Actalyke Mini II, w/ Printer, w/o Battery, "CE 2009" (110V/220V) | HELENA LABORATORIES CORPORATION | ||
41 | M52557530000 | 5753000 | Actalyke Mini II, w/ Printer, w/o Battery, "CE" (110V/220V) | HELENA LABORATORIES CORPORATION | ||
42 | 10054749000156 | 03P87-25 | 03P87-25 | Kaolin ACT CARTRIDGE | i-STAT | ABBOTT POINT OF CARE INC. |
43 | 10054749000149 | 03P86-25 | 03P86-25 | Celite ACT CARTRIDGE | i-STAT | ABBOTT POINT OF CARE INC. |