No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
---|---|---|---|---|---|---|---|---|
1 | 20884838015207 | 861287 | 861287 | MKJ | Automated external defibrillators (non-wearable) | 3 | AC Power Module | |
2 | 20884838015108 | 989803158661 | 989803158661 | MKJ | Automated external defibrillators (non-wearable) | 3 | NA | |
3 | 20884838002757 | 989803106981 | 989803106981 | MKJ | Automated external defibrillators (non-wearable) | 3 | NA | |
4 | 00884838087965 | C.02 | MSX | System, network and communication, physiological monitors | 2 | NA | ||
5 | 00884838081284 | B.01 | MSX | SYSTEM,NETWORK AND COMMUNICATION,PHYSIOLOGICAL MONITORS | 2 | NA | ||
6 | 00884838048560 | 989803160841 | 989803160841 | DXQ | blood pressure cuff | 2 | NA | |
7 | 00884838013568 | 989803172241 | 989803172241 | DSI | DETECTOR AND ALARM, ARRHYTHMIA | 2 | NA | |
8 | 00884838008939 | 989803147971 | 989803147971 | OED | Antimicrobial blood pressure cuff | 2 | NA | |
9 | 00884838082687 | 453564606171 | 453564606171 | MHX | MONITOR, PHYSIOLOGICAL, PATIENT(WITH ARRHYTHMIA DETECTION OR ALARMS) | 2 | NA | |
10 | 00884838082670 | 453564606161 | 453564606161 | MHX | MONITOR, PHYSIOLOGICAL, PATIENT(WITH ARRHYTHMIA DETECTION OR ALARMS) | 2 | NA | |
11 | 00884838082663 | 453564606151 | 453564606151 | MHX | MONITOR, PHYSIOLOGICAL, PATIENT(WITH ARRHYTHMIA DETECTION OR ALARMS) | 2 | NA | |
12 | 00884838082656 | 453564606141 | 453564606141 | MHX | MONITOR, PHYSIOLOGICAL, PATIENT(WITH ARRHYTHMIA DETECTION OR ALARMS) | 2 | NA | |
13 | 00884838082649 | 453564606131 | 453564606131 | MHX | MONITOR, PHYSIOLOGICAL, PATIENT(WITH ARRHYTHMIA DETECTION OR ALARMS) | 2 | NA | |
14 | 00884838082632 | 453564606111 | 453564606111 | MHX | MONITOR, PHYSIOLOGICAL, PATIENT(WITH ARRHYTHMIA DETECTION OR ALARMS) | 2 | NA | |
15 | 00884838048553 | 989803160831 | 989803160831 | DXQ | blood pressure cuff | 2 | NA | |
16 | 00884838048546 | 989803160821 | 989803160821 | DXQ | blood pressure cuff | 2 | NA | |
17 | 00884838048539 | 989803160811 | 989803160811 | DXQ | blood pressure cuff | 2 | NA | |
18 | 20884838015184 | 989803106971 | 989803106971 | MKJ | Automated external defibrillators (non-wearable) | 3 | NA | |
19 | 20884838003020 | 989803150401 | 989803150401 | OED | Antimicrobial blood pressure cuff | 2 | NA | |
20 | 20884838002993 | 989803150391 | 989803150391 | OED | Antimicrobial blood pressure cuff | 2 | NA | |
21 | 00884838082694 | 453564606181 | 453564606181 | MHX | MONITOR, PHYSIOLOGICAL, PATIENT(WITH ARRHYTHMIA DETECTION OR ALARMS) | 2 | NA | |
22 | 00884838099128 | CareEvent | 866435 | CareEvent is a distributed alarming solution. With CareEvent the Philips Alarm d CareEvent is a distributed alarming solution. With CareEvent the Philips Alarm distribution solution includes rules and escalation levels to deliver the right alarm to the right caregiver with the right information on a mobile device. | MSX | System, network and communication, physiological monitors | 2 | CareEvent |
23 | 00884838093973 | CS770 IntelliSpace CC & Anesthesia Upgr | 866148 | CS770 IntelliSpace Critical Care and Anesthesia Upgrade | DXJ | DISPLAY, CATHODE-RAY TUBE, MEDICAL | 2 | IntelliSpace Critical Care and Anesthesia |
24 | 00884838048577 | 989803160851 | 989803160851 | DXQ | blood pressure cuff | 2 | NA | |
25 | 00884838085565 | Intellispace CC & Anesthesia | 866148 | IntelliSpace Critical Care and Anesthesia | DXJ | DISPLAY, CATHODE-RAY TUBE, MEDICAL | 2 | IntelliSpace Critical Care and Anesthesia |
26 | 00884838083684 | 453564606081 | 453564606081 | MHX | MONITOR, PHYSIOLOGICAL, PATIENT(WITH ARRHYTHMIA DETECTION OR ALARMS) | 2 | NA | |
27 | 00884838083400 | 453564490671 | 453564490671 | MHX | MONITOR, PHYSIOLOGICAL, PATIENT(WITH ARRHYTHMIA DETECTION OR ALARMS) | 2 | NA | |
28 | 00884838082274 | 453564606121 | 453564606121 | MHX | MONITOR, PHYSIOLOGICAL, PATIENT(WITH ARRHYTHMIA DETECTION OR ALARMS) | 2 | NA | |
29 | 00884838075153 | H.02 | DXJ | DISPLAY, CATHODE-RAY TUBE, MEDICAL | 2 | NA | ||
30 | 00884838055476 | 989803192251 | 989803192251 | IKD | CABLE, ELECTRODE | 2 | NA | |
31 | 00884838055452 | 989803192231 | 989803192231 | IKD | CABLE, ELECTRODE | 2 | NA | |
32 | 00884838055421 | 989803192201 | 989803192201 | IKD | CABLE, ELECTRODE | 2 | NA | |
33 | 00884838055414 | 989803192191 | 989803192191 | IKD | CABLE, ELECTRODE | 2 | NA | |
34 | 00884838055407 | 989803192181 | 989803192181 | IKD | CABLE, ELECTRODE | 2 | NA | |
35 | 00884838053441 | A.01 | MSX | SYSTEM,NETWORK AND COMMUNICATION,PHYSIOLOGICAL MONITORS | 2 | NA | ||
36 | 00884838050099 | 989803192171 | 989803192171 | DSI | DETECTOR AND ALARM, ARRHYTHMIA | 2 | NA | |
37 | 00884838050082 | 989803191321 | 989803191321 | DSI | DETECTOR AND ALARM, ARRHYTHMIA | 2 | NA | |
38 | 00884838050068 | 989803191301 | 989803191301 | DSI | DETECTOR AND ALARM, ARRHYTHMIA | 2 | NA | |
39 | 00884838048584 | 989803160861 | 989803160861 | DXQ | blood pressure cuff | 2 | NA | |
40 | 00884838015104 | 453564106001 | 453564106001 | MKJ | Automated external defibrillators (non-wearable) | 3 | NA | |
41 | 00884838039056 | Philips SureSigns Central | 863291 | "SureSigns Central Monitoring System for connectivity to SureSigns VM patient mo "SureSigns Central Monitoring System for connectivity to SureSigns VM patient monitors, single or dual display support Includes PC with software installed, SW CD, license key, speakers, mouse, keyboard optional :printer, switch" | MHX | MONITOR, PHYSIOLOGICAL, PATIENT(WITH ARRHYTHMIA DETECTION OR ALARMS) | 2 | Philips SureSigns Central |
42 | 00884838033672 | G.00 | DXJ | DISPLAY, CATHODE-RAY TUBE, MEDICAL | 2 | NA | ||
43 | 00884838033337 | 989803163171 | 989803163171 | DXQ | blood pressure cuff | 2 | NA | |
44 | 00884838029620 | 453564606071 | 453564606071 | MHX | MONITOR, PHYSIOLOGICAL, PATIENT(WITH ARRHYTHMIA DETECTION OR ALARMS) | 2 | NA | |
45 | 00884838028388 | 863277 | 863277 | SureSigns VSi NBP/SP02/Temp/Wireless | DSK,DQA,DSA,DSJ,DXG,FLL | COMPUTER, BLOOD-PRESSURE,Oximeter,Cable, Transducer And Electrode, Patient, (Inc COMPUTER, BLOOD-PRESSURE,Oximeter,Cable, Transducer And Electrode, Patient, (Including Connector),Alarm, Blood-Pressure,Computer, Diagnostic, Pre-Programmed, Single-Function,Thermometer, Electronic, Clinical | 2 | SureSigns VSi |
46 | 00884838028906 | 863264 | 863264 | SureSigns VM1 Patient Monitor: Sp02 | MHX | MONITOR, PHYSIOLOGICAL, PATIENT(WITH ARRHYTHMIA DETECTION OR ALARMS) | 2 | SureSigns VM1 |
47 | 00884838013537 | 989803172211 | 989803172211 | DSI | DETECTOR AND ALARM, ARRHYTHMIA | 2 | NA | |
48 | 00884838028371 | 863276 | 863276 | SureSigns VSi - NBP/SPO2 | DSK,DQA,DSA,DSJ,DXG,FLL | COMPUTER, BLOOD-PRESSURE,Oximeter,Cable, Transducer And Electrode, Patient, (Inc COMPUTER, BLOOD-PRESSURE,Oximeter,Cable, Transducer And Electrode, Patient, (Including Connector),Alarm, Blood-Pressure,Computer, Diagnostic, Pre-Programmed, Single-Function,Thermometer, Electronic, Clinical | 2 | SureSigns VSi |
49 | 00884838028364 | 863275 | 863275 | SureSigns VSi - NBP | DSK,DQA,DSA,DSJ,DXG,FLL | COMPUTER, BLOOD-PRESSURE,Oximeter,Cable, Transducer And Electrode, Patient, (Inc COMPUTER, BLOOD-PRESSURE,Oximeter,Cable, Transducer And Electrode, Patient, (Including Connector),Alarm, Blood-Pressure,Computer, Diagnostic, Pre-Programmed, Single-Function,Thermometer, Electronic, Clinical | 2 | SureSigns VSi |
50 | 00884838028319 | 989803176171 | 989803176171 | IKD | CABLE, ELECTRODE | 2 | NA |
No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
---|---|---|---|---|---|---|
1 | 00853512006745 | 3603 | 3603 | 3 Lead Monitor Cable | Nikomed ECG Cable | NIKOMED USA |
2 | 00853512006707 | 3509 | 3509 | Reusable Grounding Pad Cable 10' with a Boston Scientific style connector, Non-R Reusable Grounding Pad Cable 10' with a Boston Scientific style connector, Non-REM/Non Alarm | NIKO-Surg | NIKOMED USA |
3 | 00853512006691 | 3508 | 3508 | Reusable Grounding Pad Cable 10' with a Valleylab style connector and center pin Reusable Grounding Pad Cable 10' with a Valleylab style connector and center pin (REM/Alarm) | NIKO-Surg | NIKOMED USA |
4 | 00853512006684 | 3407 | 3407 | Reusable Grounding Pad Cable 10' with a Valleylab style connector and no center Reusable Grounding Pad Cable 10' with a Valleylab style connector and no center pin (Non-REM/Non Alarm) | NIKO-Surg | NIKOMED USA |
5 | 00853512006677 | 3406 | 3406 | Reusable Grounding Pad Cable 10' with a 4mm shrouded plug connector | NIKO-Surg | NIKOMED USA |
6 | 00853512006660 | 3405 | 3405 | Reusable Grounding Pad Cable 10' with a 6mm plug connector | NIKO-Surg | NIKOMED USA |
7 | 00851797006429 | ML-0459 | Disposable Dilator KitKit Contains:ML-0444SInsulated Dilator Set, 7, 12, & 15 MM Disposable Dilator KitKit Contains:ML-0444SInsulated Dilator Set, 7, 12, & 15 MM, SterileML-0345Dilator Clip | SeaSpine | TEDAN SURGICAL INNOVATIONS, L.L.C. | |
8 | 00851530007584 | AA-LW-250-RCA | AA-LW-250-RCA | Lead Wire, 250-RCA | Avazzia | AVAZZIA INC |
9 | 00851530007577 | AA-LW-4P-RCA | AA-LW-4P-RCA | Lead Wire, 4P-RCA | Avazzia | AVAZZIA INC |
10 | 00851530007560 | AA-LW-4P-RB-B | AA-LW-4P-RB-B | Lead Wire, 4P Banana | Avazzia | AVAZZIA INC |
11 | 00851530007553 | AA-LW-2T-RB | AA-LW-2T-RB | Lead Wire, 2T-RB | Avazzia | AVAZZIA INC |
12 | 00851530007546 | AA-LW-2T-250 | AA-LW-2T-250 | Lead Wire, 2T-250 | Avazzia | AVAZZIA INC |
13 | 00851530007539 | AA-LW-4P-2T | AA-LW-4P-2T | Lead Wire, 4P-2T | Avazzia | AVAZZIA INC |
14 | 00851530007522 | AA-LW-250-130f | AA-LW-250-130f | Adapter, 250-130f | Avazzia | AVAZZIA INC |
15 | 00851530007515 | AA-LW-4P-250 | AA-LW-4P-250 | Lead Wire, 4P-250 | Avazzia | AVAZZIA INC |
16 | 00851530007508 | AA-LW-4P-250-15K | AA-LW-4P-250-15K | Attenuator, 4P-250f, 15KO | Avazzia | AVAZZIA INC |
17 | 00851530007492 | AA-LW-4P-2X-RB | AA-LW-4P-2X-RB | Lead Wire, 4P-2X-RB | Avazzia | AVAZZIA INC |
18 | 00851530007485 | AA-LW-4P-250f | AA-LW-4P-250f | Adapter, 4P-250f | Avazzia | AVAZZIA INC |
19 | 00851530007478 | AA-LW-4P-RB | AA-LW-4P-RB | Lead Wire, 4P-RB | Avazzia | AVAZZIA INC |
20 | 00851530007461 | AA-LW-130-250f | AA-LW-130-250f | Adapter, 130m-250f | Avazzia | AVAZZIA INC |
21 | 00851530007454 | AA-LW-130-RB | AA-LW-130-RB | Lead Wire, 130-RB | Avazzia | AVAZZIA INC |
22 | 00851530007447 | AA-LW-250-250-15K | AA-LW-250-250-15K | Attenuator, 250-250f-15KO | Avazzia | AVAZZIA INC |
23 | 00851530007430 | AA-LW-250-2X-250f | AA-LW-250-2X-250f | Splitter, 250-2X-250 | Avazzia | AVAZZIA INC |
24 | 00851530007423 | AA-LW-250-250 | AA-LW-250-250 | Lead Wire, 250-250 | Avazzia | AVAZZIA INC |
25 | 00851530007416 | AA-LW-250-RB | AA-LW-250-RB | Lead Wire, 250-RB | Avazzia | AVAZZIA INC |
26 | 00850018485029 | Cable | MGCBLSP | Cable, Electrode | EKG Patchâ„¢ (Cable) | NULINE SENSORS, LLC |
27 | 00850012681113 | HAR-27 | Ives MR Conditional Electrode System Harness, 27 lead wire harness, MR Unsafe (d Ives MR Conditional Electrode System Harness, 27 lead wire harness, MR Unsafe (disconnect from electrode set before CT or MR imaging) | Ives EEG Solutions | IVES EEG SOLUTIONS, LLC | |
28 | 00850012681106 | HAR-25 | Ives MR Conditional Electrode System Harness, 25 lead wire harness, MR Unsafe (d Ives MR Conditional Electrode System Harness, 25 lead wire harness, MR Unsafe (disconnect from electrode set before CT or MR imaging) | Ives EEG Solutions | IVES EEG SOLUTIONS, LLC | |
29 | 00850012681090 | HAR-23 | Ives MR Conditional Electrode System Harness, 23 lead wire harness, MR Unsafe (d Ives MR Conditional Electrode System Harness, 23 lead wire harness, MR Unsafe (disconnect from electrode set before CT or MR imaging) | Ives EEG Solutions | IVES EEG SOLUTIONS, LLC | |
30 | 00850012681083 | HAR-21 | Ives MR Conditional Electrode System Harness, 21 lead wire harness, MR Unsafe (d Ives MR Conditional Electrode System Harness, 21 lead wire harness, MR Unsafe (disconnect from electrode set before CT or MR imaging) | Ives EEG Solutions | IVES EEG SOLUTIONS, LLC | |
31 | 00850011306505 | 5.38 m | 31-0202-0005 | Flexible cable to connect the High Density Junction Box to the ATLAS Neurophysio Flexible cable to connect the High Density Junction Box to the ATLAS Neurophysiology System. | High Density Tether 5.38 m | NEURALYNX, INC. |
32 | 00850011306499 | 31-0602-0033 | ADPT-HD-Y Adapter Cable for use with the ATLAS Neurophysiology System. | ADPT-HD-Y Adapter Cable | NEURALYNX, INC. | |
33 | 00850011306475 | 3m | The High Density Tether is a flexible cable to connect the High Density Junction The High Density Tether is a flexible cable to connect the High Density Junction Box to the ATLAS Neurophysiology System. The High Density Tether is a component of the ATLAS Neurophysiology System. | High Density Tether 3m | NEURALYNX, INC. | |
34 | 00850011306468 | 2m | 31-0202-0003 | The High Density Tether is a flexible cable to connect the High Density Junction The High Density Tether is a flexible cable to connect the High Density Junction Box to the ATLAS Neurophysiology System. The High Density Tether is a component of the ATLAS Neurophysiology System. | High Density Tether 2m | NEURALYNX, INC. |
35 | 00850011306451 | 1m | 31-0202-0002 | The High Density Tether is a flexible cable to connect the High Density Junction The High Density Tether is a flexible cable to connect the High Density Junction Box to the ATLAS Neurophysiology System. The High Density Tether is a component of the ATLAS Neurophysiology System. | High Density Tether 1m | NEURALYNX, INC. |
36 | 00850011306444 | -H | 31-0602-0040 | Passive adapter with touchproof inputs and a high density output for adapting 3r Passive adapter with touchproof inputs and a high density output for adapting 3rd party electrode interface cables to the ATLAS Neurophysiology System. Version "H" is labeled for connections to electrodes 449-512. | High Density Junction Box - H | NEURALYNX, INC. |
37 | 00850011306437 | -G | 31-0602-0039 | Passive adapter with touchproof inputs and a high density output for adapting 3r Passive adapter with touchproof inputs and a high density output for adapting 3rd party electrode interface cables to the ATLAS Neurophysiology System. Version "G" is labeled for connections to electrodes 385-448. | High Density Junction Box - G | NEURALYNX, INC. |
38 | 00850011306420 | -F | 31-0602-0038 | Passive adapter with touchproof inputs and a high density output for adapting 3r Passive adapter with touchproof inputs and a high density output for adapting 3rd party electrode interface cables to the ATLAS Neurophysiology System. Version "F" is labeled for connections to electrodes 321-384. | High Density Junction Box - F | NEURALYNX, INC. |
39 | 00850011306413 | -E | 31-0602-0037 | Passive adapter with touchproof inputs and a high density output for adapting 3r Passive adapter with touchproof inputs and a high density output for adapting 3rd party electrode interface cables to the ATLAS Neurophysiology System. Version "E" is labeled for connections to electrodes 257-320. | High Density Junction Box - E | NEURALYNX, INC. |
40 | 00850011306406 | -D | 31-0602-0036 | Passive adapter with touchproof inputs and a high density output for adapting 3r Passive adapter with touchproof inputs and a high density output for adapting 3rd party electrode interface cables to the ATLAS Neurophysiology System. Version "D" is labeled for connections to electrodes 193-256. | High Density Junction Box - D | NEURALYNX, INC. |
41 | 00850011306390 | -C | 31-0602-0035 | Passive adapter with touchproof inputs and a high density output for adapting 3r Passive adapter with touchproof inputs and a high density output for adapting 3rd party electrode interface cables to the ATLAS Neurophysiology System. Version "C" is labeled for connections to electrodes 129-192. | High Density Junction Box - C | NEURALYNX, INC. |
42 | 00850011306383 | -B | 31-0602-0034 | Passive adapter with touchproof inputs and a high density output for adapting 3r Passive adapter with touchproof inputs and a high density output for adapting 3rd party electrode interface cables to the ATLAS Neurophysiology System. Version "B" is labeled for connections to electrodes 65-128. | High Density Junction Box - B | NEURALYNX, INC. |
43 | 00850011306192 | ATLAS Patient Event Marker | Patient Event Marker | The ATLAS Patient Event Marker is an optional configuration of the ATLAS Neuroph The ATLAS Patient Event Marker is an optional configuration of the ATLAS Neurophysiology System that allows the patient to mark an event in the Data Acquisition Software. | ATLAS Patient Event Marker | NEURALYNX, INC. |
44 | 00850011214374 | PMI52-00548 | PMI52-00548 | MONOPOLAR CABLE MALE BANANA/MALE BOVIE | ELMED | PROGRESSIVE MEDICAL INSTRUMENTATION INC |
45 | 00850011214312 | PMI52-00546 | PMI52-00546 | BIPOLAR CABLE DUAL BANANA/2 PIN | ELMED | PROGRESSIVE MEDICAL INSTRUMENTATION INC |
46 | 00850011214305 | PMI52-00532 | PMI52-00532 | MONOPOLAR CABLE 10 FEET | ELMED | PROGRESSIVE MEDICAL INSTRUMENTATION INC |
47 | 00850011214251 | PMI5023 | PMI5023 | MONOPOLAR CABLE WITH OLSEN & BOVIE PLUGS | ELMED | PROGRESSIVE MEDICAL INSTRUMENTATION INC |
48 | 00843059122916 | 48755028 | LEAD, EXTENSION BLUE 183 CM / 72 IN | Stryker | TEDAN SURGICAL INNOVATIONS, L.L.C. | |
49 | 00843059122909 | 48755018 | LEAD, CROCODILE CLIP, 122 CM / 48 IN | Stryker | TEDAN SURGICAL INNOVATIONS, L.L.C. | |
50 | 00843059117745 | ZS-0345 | DILATOR CLIP, STERILE, SINGLE USE | Zimmer | TEDAN SURGICAL INNOVATIONS, L.L.C. |