No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
---|---|---|---|---|---|---|---|---|
1 | 00888912402996 | 79977 | KIT HIVOLT PROBE | IPF | Stimulator, muscle, powered | 2 | CHATTANOOGA | |
2 | 00888912022330 | 3013 | BARIATRC VF DISP CLF CF ASY PR | JOW | SLEEVE, LIMB, COMPRESSIBLE | 2 | AIRCAST | |
3 | 00888912008549 | 11B01 | LARGE KNEE CUFF ONLY | ILO | Pack, hot or cold, water circulating | 2 | AIRCAST | |
4 | 00888912006675 | 11-1522 | ICEMAN, ANKLE COLD PAD | ILO | Pack, hot or cold, water circulating | 2 | DONJOY | |
5 | 00190446703457 | 88-040000048494 | XTender Long | ITQ | JOINT, KNEE, EXTERNAL BRACE | 1 | NON FRANCHISE | |
6 | 00888912025362 | 78046 | APPLICATOR 10CM ASSY | IMI | Ultrasonic diathermy for use in applying therapeutic deep heat | 2 | CHATTANOOGA | |
7 | 00888912348669 | 4767 | KIT TRITON DTS PKG INT'L STD | ITH | EQUIPMENT, TRACTION, POWERED | 2 | CHATTANOOGA | |
8 | 00888912292122 | 27376 | KIT LEAD 2CH EPR | IKD | CABLE, ELECTRODE | 2 | CHATTANOOGA | |
9 | 00888912022460 | 30A | VENAFLOW SYSTEM | JOW | SLEEVE, LIMB, COMPRESSIBLE | 2 | AIRCAST | |
10 | 00888912000154 | 1033 | THERATHERM MOISTHEAT PAD SHLDR | IRT | PAD, HEATING, POWERED | 2 | CHATTANOOGA | |
11 | 00190446660330 | 155-79-84027 | ARM SLING, CTN/POLY LG | ILI | SLING, ARM | 1 | PROCARE | |
12 | 00190446660323 | 155-79-84025 | ARM SLING, CTN/POLY MED | ILI | SLING, ARM | 1 | PROCARE | |
13 | 00190446660316 | 155-79-84023 | ARM SLING, CTN/POLY SM | ILI | SLING, ARM | 1 | PROCARE | |
14 | 00190446660309 | 155-79-84022 | ARM SLING, CTN/POLY XSM | ILI | SLING, ARM | 1 | PROCARE | |
15 | 00190446714033 | 88-814000004021 | U2 WRIST UNIV LT | ITQ | JOINT, KNEE, EXTERNAL BRACE | 1 | NON FRANCHISE | |
16 | 00888912026932 | 79-80090 | 16 CKD KNEE IMMOBILIZER | MHW | Dressing, compression | 1 | PROCARE | |
17 | 00888912026321 | 79-72273 | PRO HEEL CUPS/PAIR - SMALL | KYS | INSOLES, MEDICAL | 1 | PROCARE | |
18 | 00190446708223 | 88-578000370513 | WRIST/HAND ORTHOSIS, BLK, L LT | ITQ | JOINT, KNEE, EXTERNAL BRACE | 1 | NON FRANCHISE | |
19 | 00190446708216 | 88-578000370512 | WRIST/HAND ORTHOSIS, BLK, M LT | ITQ | JOINT, KNEE, EXTERNAL BRACE | 1 | NON FRANCHISE | |
20 | 00190446708209 | 88-578000370511 | WRIST/HAND ORTHOSIS, BLK, S LT | ITQ | JOINT, KNEE, EXTERNAL BRACE | 1 | NON FRANCHISE | |
21 | 00190446708155 | 88-578000370501 | WRIST/HAND ORTHOSIS, BLK, S RT | ITQ | JOINT, KNEE, EXTERNAL BRACE | 1 | NON FRANCHISE | |
22 | 00190446707783 | 88-578000370534 | Wrist Hand Thumb Orthosis XL LT | ITQ | JOINT, KNEE, EXTERNAL BRACE | 1 | NON FRANCHISE | |
23 | 00190446707745 | 88-578000370530 | Wrist Hand Thumb Orthosis XS LT | ITQ | JOINT, KNEE, EXTERNAL BRACE | 1 | NON FRANCHISE | |
24 | 00190446707691 | 88-578000370520 | Wrist Hand Thumb Orthosis XS RT | ITQ | JOINT, KNEE, EXTERNAL BRACE | 1 | NON FRANCHISE | |
25 | 00190446707417 | 88-578000372071 | Ulnar Splint S | ITQ | JOINT, KNEE, EXTERNAL BRACE | 1 | NON FRANCHISE | |
26 | 00190446662709 | 155-79-81235 | SHOE, POST-OP SQ TOE MED | KNP | ORTHOSIS, CORRECTIVE SHOE | 1 | PROCARE | |
27 | 00190446662693 | 155-79-81233 | SHOE, POST-OP SQ TOE SM | KNP | ORTHOSIS, CORRECTIVE SHOE | 1 | PROCARE | |
28 | 00190446660552 | 155-79-96024 | KNEE IMMOBILIZER, XL 24 IN | ITQ | JOINT, KNEE, EXTERNAL BRACE | 1 | PROCARE | |
29 | 00190446660538 | 155-79-96019 | KNEE IMMOBILIZER, XL 20 IN | ITQ | JOINT, KNEE, EXTERNAL BRACE | 1 | PROCARE | |
30 | 00190446660521 | 155-79-96018 | KNEE IMMOBILIZER, XL 18 IN | ITQ | JOINT, KNEE, EXTERNAL BRACE | 1 | PROCARE | |
31 | 00190446660514 | 155-79-96016 | KNEE IMMOBILIZER, UNIV 16 IN | ITQ | JOINT, KNEE, EXTERNAL BRACE | 1 | PROCARE | |
32 | 00190446660507 | 155-79-96014 | KNEE IMMOBILIZER, UNIV 14 IN | ITQ | JOINT, KNEE, EXTERNAL BRACE | 1 | PROCARE | |
33 | 00190446660491 | 155-79-96012 | KNEE IMMOBILIZER, UNIV 12 IN | ITQ | JOINT, KNEE, EXTERNAL BRACE | 1 | PROCARE | |
34 | 00190446660347 | 155-79-84028 | ARM SLING, CTN/POLY XLG | ILI | SLING, ARM | 1 | PROCARE | |
35 | 00190446714224 | 88-004000041214 | CONFRMR I DIAB BOOT,1CUF,RT,XXL | ITQ | JOINT, KNEE, EXTERNAL BRACE | 1 | NON FRANCHISE | |
36 | 00190446714125 | 88-814000000019 | Universal Arm Sling with Foam Strap Adult | ITQ | JOINT, KNEE, EXTERNAL BRACE | 1 | NON FRANCHISE | |
37 | 00190446714040 | 88-814000004020 | U2 WRIST UNIV RT | ITQ | JOINT, KNEE, EXTERNAL BRACE | 1 | NON FRANCHISE | |
38 | 00190446713968 | 88-814000006295 | HKO ANTERIOR CLOSURE KNEE XL | ITQ | JOINT, KNEE, EXTERNAL BRACE | 1 | NON FRANCHISE | |
39 | 00190446713586 | 88-814000006293 | HKO ANTERIOR CLOSURE KNEE MD | ITQ | JOINT, KNEE, EXTERNAL BRACE | 1 | NON FRANCHISE | |
40 | 00190446713579 | 88-814000006292 | HKO ANTERIOR CLOSURE KNEE SM | ITQ | JOINT, KNEE, EXTERNAL BRACE | 1 | NON FRANCHISE | |
41 | 00190446713548 | 88-814008144803 | BAKER PLANTAR FASCIITIS NIGHT SPLINT, MEDIUM | ITQ | JOINT, KNEE, EXTERNAL BRACE | 1 | NON FRANCHISE | |
42 | 00190446713517 | 88-814008144802 | BAKER PLANTAR FASCIITIS NIGHT SPLINT, SMALL | ITQ | JOINT, KNEE, EXTERNAL BRACE | 1 | NON FRANCHISE | |
43 | 00190446707134 | 88-578000883065 | ELBOW SLEEVE W/PAD, 1/8, LARGE | ITQ | JOINT, KNEE, EXTERNAL BRACE | 1 | NON FRANCHISE | |
44 | 00190446707004 | 88-578000994303 | Soft Heel Cushions L | ITQ | JOINT, KNEE, EXTERNAL BRACE | 1 | NON FRANCHISE | |
45 | 00190446706991 | 88-578000994302 | Soft Heel Cushions M | ITQ | JOINT, KNEE, EXTERNAL BRACE | 1 | NON FRANCHISE | |
46 | 00190446706977 | 88-578000994301 | Soft Heel Cushions S | ITQ | JOINT, KNEE, EXTERNAL BRACE | 1 | NON FRANCHISE | |
47 | 00190446705888 | 88-578000372183 | MID LENGTH HUMERAL SPLINT, LARGE | ITQ | JOINT, KNEE, EXTERNAL BRACE | 1 | NON FRANCHISE | |
48 | 00190446705734 | 88-578000751015 | ANKLE STIRRUP W/AIR LINER BLK | ITQ | JOINT, KNEE, EXTERNAL BRACE | 1 | NON FRANCHISE | |
49 | 00190446705000 | 88-578000372163 | Extended Length Humeral Splint L | ITQ | JOINT, KNEE, EXTERNAL BRACE | 1 | NON FRANCHISE | |
50 | 00190446704997 | 88-578000372162 | Extended Length Humeral Splint M | ITQ | JOINT, KNEE, EXTERNAL BRACE | 1 | NON FRANCHISE |
No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
---|---|---|---|---|---|---|
1 | 08050040997329 | UBHS-02 | 654300-9003 | Replacement Power Supply, Accelstim 4300 | Accelstim | IGEA SPA |
2 | 08050040997312 | UBHS-02 | 654300-8002 | Replacement Transducer Holder, Accelstim 4300 | Accelstim | IGEA SPA |
3 | 08050040997305 | UBHS-02 | 654300-8001 | Replacement Strap, Accelstim 4300 | Accelstim | IGEA SPA |
4 | 08050040997299 | UBHS-02 | 654300-9001 | Replacement Ultrasound Gel, Accelstim 4300 | Accelstim | IGEA SPA |
5 | 08050040997213 | UBHS-02 | 4300 | Bone Growth Stimulator | AccelStim | IGEA SPA |
6 | 00888912220972 | 11-9102 | KIT,EXTN BELT,SPINALOGIC ECOIL | CMF | DJO, LLC | |
7 | 00888912217163 | 11-1520 | KIT,SOFTGOODS,SPINALOGIC ECOIL | CMF | DJO, LLC | |
8 | 00888912161770 | OL1000 Single Coil Size 4 | 01-211-0004 | The OL1000 and OL1000 SC BONE GROWTH STIMULATORS are indicated for the noninvasi The OL1000 and OL1000 SC BONE GROWTH STIMULATORS are indicated for the noninvasive treatment of an established nonunion acquired secondary to trauma, excluding vertebrae and all flat bones. A nonunion is considered to be established when the fracture site shows no visibly progressive signs of healing.The OL1000 and OL1000 SC are portable, battery powered, microprocessor-controlled, noninvasive bone growth stimulators. The device is worn by a patient for 30 minutes a day and provides local electromagnetic field treatment for a non-healing fracture. The device produces very low energy combined static and dynamic electromagnetic fields on the order of the earth’s magnetic field. The device has a push button that starts the treatment and an audible tone to notify the patient that a treatment has started or has ended. A liquid crystal display (LCD) is utilized to display the status of the device, e.g., treatment record, daily treatment time countdown. | CMF | DJO, LLC |
9 | 00888912161763 | OL1000 Single Coil Size 3 | 01-211-0003 | The OL1000 and OL1000 SC BONE GROWTH STIMULATORS are indicated for the noninvasi The OL1000 and OL1000 SC BONE GROWTH STIMULATORS are indicated for the noninvasive treatment of an established nonunion acquired secondary to trauma, excluding vertebrae and all flat bones. A nonunion is considered to be established when the fracture site shows no visibly progressive signs of healing.The OL1000 and OL1000 SC are portable, battery powered, microprocessor-controlled, noninvasive bone growth stimulators. The device is worn by a patient for 30 minutes a day and provides local electromagnetic field treatment for a non-healing fracture. The device produces very low energy combined static and dynamic electromagnetic fields on the order of the earth’s magnetic field. The device has a push button that starts the treatment and an audible tone to notify the patient that a treatment has started or has ended. A liquid crystal display (LCD) is utilized to display the status of the device, e.g., treatment record, daily treatment time countdown. | CMF | DJO, LLC |
10 | 00888912161756 | OL1000 Single Coil Size 2 | 01-211-0002 | The OL1000 and OL1000 SC BONE GROWTH STIMULATORS are indicated for the noninvasi The OL1000 and OL1000 SC BONE GROWTH STIMULATORS are indicated for the noninvasive treatment of an established nonunion acquired secondary to trauma, excluding vertebrae and all flat bones. A nonunion is considered to be established when the fracture site shows no visibly progressive signs of healing.The OL1000 and OL1000 SC are portable, battery powered, microprocessor-controlled, noninvasive bone growth stimulators. The device is worn by a patient for 30 minutes a day and provides local electromagnetic field treatment for a non-healing fracture. The device produces very low energy combined static and dynamic electromagnetic fields on the order of the earth’s magnetic field. The device has a push button that starts the treatment and an audible tone to notify the patient that a treatment has started or has ended. A liquid crystal display (LCD) is utilized to display the status of the device, e.g., treatment record, daily treatment time countdown. | CMF | DJO, LLC |
11 | 00888912161749 | OL1000 Single Coil Size 1 | 01-211-0001 | The OL1000 and OL1000 SC BONE GROWTH STIMULATORS are indicated for the noninvasi The OL1000 and OL1000 SC BONE GROWTH STIMULATORS are indicated for the noninvasive treatment of an established nonunion acquired secondary to trauma, excluding vertebrae and all flat bones. A nonunion is considered to be established when the fracture site shows no visibly progressive signs of healing.The OL1000 and OL1000 SC are portable, battery powered, microprocessor-controlled, noninvasive bone growth stimulators. The device is worn by a patient for 30 minutes a day and provides local electromagnetic field treatment for a non-healing fracture. The device produces very low energy combined static and dynamic electromagnetic fields on the order of the earth’s magnetic field. The device has a push button that starts the treatment and an audible tone to notify the patient that a treatment has started or has ended. A liquid crystal display (LCD) is utilized to display the status of the device, e.g., treatment record, daily treatment time countdown. | CMF | DJO, LLC |
12 | 00888912011495 | Spinalogic | 01-207-0007 | The SpinaLogic is a portable, battery powered, microcontrolled, noninvasive bone The SpinaLogic is a portable, battery powered, microcontrolled, noninvasive bone growth stimulator indicated as an adjunct electrical treatment to primary lumbar spinal fusion surgery for one or two levels. The SpinaLogic is available in one size. | CMF | DJO, LLC |
13 | 00888912011488 | OL1000 Dual Coil | 01-203-0001 | The OL1000 and OL1000 SC BONE GROWTH STIMULATORS are indicated for the noninvasi The OL1000 and OL1000 SC BONE GROWTH STIMULATORS are indicated for the noninvasive treatment of an established nonunion acquired secondary to trauma, excluding vertebrae and all flat bones. A nonunion is considered to be established when the fracture site shows no visibly progressive signs of healing.The OL1000 and OL1000 SC are portable, battery powered, microprocessor-controlled, noninvasive bone growth stimulators. The device is worn by a patient for 30 minutes a day and provides local electromagnetic field treatment for a non-healing fracture. The device produces very low energy combined static and dynamic electromagnetic fields on the order of the earth’s magnetic field. The device has a push button that starts the treatment and an audible tone to notify the patient that a treatment has started or has ended. A liquid crystal display (LCD) is utilized to display the status of the device, e.g., treatment record, daily treatment time countdown. | CMF | DJO, LLC |
14 | 00887868269318 | 1067718-72 | 1067718-72 | Biomet OrthoPak Non-invasive Bone Growth Stimulator System | EBI, LLC | |
15 | 00887868269301 | 1067718-63 | 1067718-63 | Biomet OrthoPak Non-invasive Bone Growth Stimulator System | EBI, LLC | |
16 | 00887868269295 | 1067718-45 | 1067718-45 | Biomet OrthoPak Non-invasive Bone Growth Stimulator System | EBI, LLC | |
17 | 00887868269288 | 1067716-72 | 1067716-72 | Biomet SpinalPak Non-invasive Spine Fusion Stimulator System | EBI, LLC | |
18 | 00887868269271 | 1067716-63 | 1067716-63 | Biomet SpinalPak Non-invasive Spine Fusion Stimulator System | EBI, LLC | |
19 | 00887868269264 | 1067716-45 | 1067716-45 | Biomet SpinalPak Non-invasive Spine Fusion Stimulator System | EBI, LLC | |
20 | 00880304820852 | 106130-22 | 106130-22 | ELECTRODES, 63B, SPINALPAK/ORTHOPAK | Biomet SpinalPak / OrthoPak | EBI, LLC |
21 | 00880304820845 | 106130-14 | 106130-14 | BELT EXTENSION, LARGE, SPINALPAK | Biomet SpinalPak / OrthoPak | EBI, LLC |
22 | 00850372007264 | 1101-0001-R | 1101-0001-R | ActaStim-S Spine Fusion Stimulator Replacement Generator | ActaStim-S | THERAGEN, LLC |
23 | 00850372007257 | 4101-0002 | ActaStim-S Spine Fusion Stimulator - Shower Covers, Electrode | ActaStim-S | THERAGEN, LLC | |
24 | 00850372007240 | 1101-0000 | 1101-0000 | ActaStim-S Spine Fusion Stimulator System | ActaStim-S | THERAGEN, LLC |
25 | 00850372007233 | 1101-0016 | 1101-0016 | ActaStim-S Spine Fusion Stimulator - Dock, Battery Charger | ActaStim-S | THERAGEN, LLC |
26 | 00850372007226 | 1101-0003 | 1101-0003 | ActStim-S Spine Fusion Stimulator Charger | ActaStim-S | THERAGEN, LLC |
27 | 00850372007219 | 4101-0001 | 4101-0001 | ActaStim-S Spine Fusion Stimulator - Electrodes, Type 2 | ActaStim-S | THERAGEN, LLC |
28 | 00850372007202 | 4101-0000 | 4101-0000 | ActaStim-S Spine Fusion Stimulator - Electrodes, Type 1 | ActaStim-S | THERAGEN, LLC |
29 | 00850372007196 | 1101-0006 | 1101-0006 | ActaStim-S Spine Fusion Stimulator - Leadwire, Short | ActaStim-S | THERAGEN, LLC |
30 | 00850372007189 | 1101-0007 | 1101-0007 | ActaStim-S Spine Fusion Stimulator - Leadwire, Long | ActaStim-S | THERAGEN, LLC |
31 | 00850372007172 | 1101-0002 | 1101-0002 | ActaStim-S Spine Fusion Stimulator Battery | ActaStim-S | THERAGEN, LLC |
32 | 00850372007165 | 1101-0001 | 1101-0001 | ActaStim-S Spine Fusion Stimulator Generator | ActaStim-S | THERAGEN, LLC |
33 | 00812301020676 | 1068339 | 1068339 | BHS DEMO UNITBiomet EBI Bone Healing SystemDemonstration Unit Not For Human Use | Biomet EBI Bone Healing System | EBI, LLC |
34 | 00812301020669 | 1068317 | 1068317 | International Wall Plug Adapter Kit | Biomet Bone Healing System | EBI, LLC |
35 | 00812301020652 | 1068315 | 1068315 | WALL AC ADAPTER | Biomet EBI Bone Healing System | EBI, LLC |
36 | 00812301020645 | 1068314 | 1068314 | STRAP, SFLX CLAVICLE COILETE | Biomet EBI Bone Healing System | EBI, LLC |
37 | 00812301020638 | 1068313 | 1068313 | STRAP, SFLX STANDARD COILETTE | Biomet EBI Bone Healing System | EBI, LLC |
38 | 00812301020621 | 1068240 | 1068240 | SFLX - XL COILETTE | Biomet EBI Bone Healing System | EBI, LLC |
39 | 00812301020614 | 1068239 | 1068239 | SFLX - MINI COILETTE | Biomet EBI Bone Healing System | EBI, LLC |
40 | 00812301020607 | 1068238 | 1068238 | SFLX - COILETTE | Biomet EBI Bone Healing System | EBI, LLC |
41 | 00812301020591 | 1068237 | 1068237 | SFLX 4-4 COIL | Biomet EBI Bone Healing System | EBI, LLC |
42 | 00812301020584 | 1068236 | 1068236 | SFLX 4-1 COIL | Biomet EBI Bone Healing System | EBI, LLC |
43 | 00812301020577 | 1068235 | 1068235 | SFLX 4 COIL | Biomet EBI Bone Healing System | EBI, LLC |
44 | 00812301020560 | 1068234 | 1068234 | BIOMET EBI BONE HEALING SYSTEM | Biomet EBI Bone Healing System | EBI, LLC |
45 | 00812301020553 | 1068233 | 1068233 | CONTROLLER ASSEMBLY, REPLACEMENT - BIOMET EBI BONE HEALING SYSTEM | Biomet EBI Bone Healing System | EBI, LLC |
46 | 00812301020546 | 1068229 | 1068229 | SFLX 3 COIL | Biomet EBI Bone Healing System | EBI, LLC |
47 | 00812301020539 | 1068228 | 1068228 | SFLX 2-4 COIL | Biomet EBI Bone Healing System | EBI, LLC |
48 | 00812301020522 | 1068227 | 1068227 | SFLX 2-1 COIL | Biomet EBI Bone Healing System | EBI, LLC |
49 | 00812301020515 | 1068226 | 1068226 | SFLX 5 COIL | Biomet EBI Bone Healing System | EBI, LLC |
50 | 00812301020508 | 1068225 | 1068225 | SFLX 1 COIL | Biomet EBI Bone Healing System | EBI, LLC |