| No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
|---|---|---|---|---|---|---|---|---|
| 1 | 00885074459639 | 8361234 | SCREW REMOVAL | FSM | TRAY, SURGICAL, INSTRUMENT | 1 | n/a | |
| 2 | 00885074378404 | 9960136 | DISTRACTOR 9960136 TLIF | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | N/A | |
| 3 | 00885074351087 | 1701188R | TSRH-3D IMPLANT TRAY | FSM | TRAY, SURGICAL, INSTRUMENT | 1 | N/A | |
| 4 | 00885074154527 | 8670016 | PAK KIT LOANER TRAY | FSM | TRAY, SURGICAL, INSTRUMENT | 1 | N/A | |
| 5 | 00885074087801 | 2940352 | INSTRUMENT 2940352 11MM SHAVER | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | N/A | |
| 6 | 00885074034089 | 7480885 | INSTRUMENT 7480885 8.5MM TAP | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | N/A | |
| 7 | 00763000361204 | EX0220004 | HOLDER EX0220004 BLADE | GAD | RETRACTOR | 1 | n/a | |
| 8 | 00763000205256 | 9010009001 | DRIVER 9010009001 T27 SET SCREW DRIVER | HXX | SCREWDRIVER | 1 | n/a | |
| 9 | 00763000191818 | X0518057 | INSERTER X0518057 SOVEREIGN RED PROFILE | MAX,OVD | Intervertebral fusion device with bone graft, lumbar,Intervertebral fusion devic Intervertebral fusion device with bone graft, lumbar,Intervertebral fusion device with integrated fixation, lumbar | 2 | N/A | |
| 10 | 00763000140021 | 9564030 | DILATOR 9564030 MICRO | GAD | RETRACTOR | 1 | NA | |
| 11 | 00721902974793 | 6971114 | INSTRUMENT 6971114 MALLET | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | N/A | |
| 12 | 00763000036331 | 9450051 | DISPOSABLE 9450051 NIM 2.3MM BLL TIP PRB | ETN | STIMULATOR, NERVE | 2 | N/A | |
| 13 | 00721902983849 | 9198903 | CASE 9198903 INS LOWER TRAY 1 | FSM | TRAY, SURGICAL, INSTRUMENT | 1 | n/a | |
| 14 | 00721902725913 | X8683509 | INSTRUMENT X8683509 THOR TAP 3 5MM | HWX | TAP, BONE | 1 | N/A | |
| 15 | 00721902689611 | 185-460L | LID 185-460L GENERIC 1/2 TRAY | FSM | TRAY, SURGICAL, INSTRUMENT | 1 | N/A | |
| 16 | 00721902648236 | 8161020 | INSTRUMENT 8161020 S 2PRNG STPL HLDR | MNI,KWQ,KWP,MNH | ORTHOSIS, SPINAL PEDICLE FIXATION,APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BOD ORTHOSIS, SPINAL PEDICLE FIXATION,APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY,APPLIANCE, FIXATION, SPINAL INTERLAMINAL,Orthosis, spondylolisthesis spinal fixation | 2 | N/A | |
| 17 | 00681490902939 | 8691016 | INSTRUMENT 8691016 CRSLK MSR TL CRD 19MM | HWT | TEMPLATE | 1 | N/A | |
| 18 | 00681490002387 | Y895-I16FO | REAMER | HTO | REAMER | 1 | Medtronic Reusable Instruments | |
| 19 | 00673978141268 | X0598-006 | WIRE X0598-006 30 NON-THREAD UCSS WIRE | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | N/A | |
| 20 | 00673978072395 | 890-501 | INSTRUMENT 890-501 REMOVER LARGE | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | N/A | |
| 21 | 00673978070841 | 876-468 | INSTRUMENT 876-468 DEPTH GAUGE | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | N/A | |
| 22 | 00673978069050 | 875-078 | INSTRUMENT 875-078 14MM DISTRACTOR PINS | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | N/A | |
| 23 | 00673978050515 | 836-018 | INSTRUMENT 836-018 SOLID TAP 7.5MM | HWX | TAP, BONE | 1 | N/A | |
| 24 | 00673978011394 | 185-064 | CASE 185-064 CD HORIZON BASELID STEAM | FSM | TRAY, SURGICAL, INSTRUMENT | 1 | N/A | |
| 25 | 00643169997134 | EX0317034 | RASP EX0317034 15DEG | HTR | RASP | 1 | n/a | |
| 26 | 00643169791473 | EX0316012 | RETRACTOR EX0316012 TRIMLINE | GAD | RETRACTOR | 1 | N/A | |
| 27 | 00643169766815 | EX0416033 | PIN EX0416033 PLATE HOLDING | FZX | Guide, surgical, instrument | 1 | N/A | |
| 28 | 00643169762022 | EX0416028 | INSERTER EX0416028 STRAIGHT BONE | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | N/A | |
| 29 | 00643169672840 | NAV2080K | TAP NAV2080K VERT TAP 4.5MM | OLO | Orthopedic stereotaxic instrument | 2 | N/A | |
| 30 | 00643169662988 | X0815035 | RETRACTOR X0815035 22MMX5CM ANG TUBULAR | GAD | RETRACTOR | 1 | n/a | |
| 31 | 00643169591431 | EX0115004 | BAR EX0115004 T | HWT | TEMPLATE | 1 | N/A | |
| 32 | 00643169546875 | 9735468 | TAPS MODULE SET 9735468 MODULE AND LID | OLO | Orthopedic stereotaxic instrument | 2 | N/A | |
| 33 | 00643169526013 | X0614034 | INSERTER X0614034 GRAFT | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | N/A | |
| 34 | 00643169453487 | EX0114070 | FORK EX0114070 ALIGNMENT | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | N/A | |
| 35 | 00643169442047 | X1113036 | SPREADER X1113036 6MM CAM | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | N/A | |
| 36 | 00643169400238 | EX0713147 | DISTRACTOR EX0713147 5MM | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | N/A | |
| 37 | 00643169347878 | 3004986 | TEMPLATE 3004986 ZEVO 86MM 4 LVL | HWT | TEMPLATE | 1 | N/A | |
| 38 | 00643169328358 | 3004967 | TEMPLATE 3004967 ZEVO 67MM 4 LVL | HWT | TEMPLATE | 1 | N/A | |
| 39 | 00643169290204 | 5485914 | HANDLE 5485914 ARI LATERAL HANDLE | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | N/A | |
| 40 | 00643169273542 | EX0812922 | COUNTER EX0812922 TORQUE 5.5/6.0 CLOSED | HXC,LXH | WRENCH,Orthopedic manual surgical instrument | 1 | n/a | |
| 41 | 00643169272842 | 5619013 | TEMPLATE 5619013 6.0X6.9MM PK RD90-130MM | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | N/A | |
| 42 | 00643169246775 | EX0812928 | SPREADER EX0812928 LAMINAR | LXH | Orthopedic manual surgical instrument | 1 | n/a | |
| 43 | 00643169029170 | 5584134 | REDUCER 5584134 CDHS 5.5/6.0 BEALE SLOTS | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | N/A | |
| 44 | 00643169027046 | EX0511080 | RASP EX0511080 BAYONET HEAD 8MM X 20MM | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | N/A | |
| 45 | 00643169019942 | 7069039 | LID 7069039 CDHS 5.5/6.0 SET SCREW MOD | FSM | TRAY, SURGICAL, INSTRUMENT | 1 | N/A | |
| 46 | 00613994993816 | 7069034 | TRAY 7069034 CDHS 5.5 INSTRUMENT 3 LOWER | FSM | TRAY, SURGICAL, INSTRUMENT | 1 | N/A | |
| 47 | 00613994980045 | 7069001 | TRAY 7069001 SEXTANT RODS | FSM | TRAY, SURGICAL, INSTRUMENT | 1 | N/A | |
| 48 | 00613994946614 | 5484338 | STARTER 5484338 NON-BREAKOFF PLUG | HXX | SCREWDRIVER | 1 | N/A | |
| 49 | 00613994888372 | 9396009 | TRAY 9396009 INSTTRAY3 | MQP | SPINAL VERTEBRAL BODY REPLACEMENT DEVICE | 2 | N/A | |
| 50 | 00613994880390 | 1855121 | LID 1855121 4.75 OUS EXTRA SCRW MOD LID | FSM | TRAY, SURGICAL, INSTRUMENT | 1 | N/A |
| No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
|---|---|---|---|---|---|---|
| 1 | B330OT02240 | OT-0224 | The Osseoflex® SB is designed for use in balloon kyphoplasty. The balloon serves The Osseoflex® SB is designed for use in balloon kyphoplasty. The balloon serves to create a cavity in the vertebral body, thereby reducing the fracture while still allowing for cement interdigitation. The balloon catheter is the functional part of the device that creates a cavity and reduces the fracture. The balloon catheter provides a conduit through which the physician can inflate the balloon at the distal end of the catheter. After the bone is disrupted, PMMA is injected through an Osseoflex® SN steerable needle to fill the previously created void(s).An access channel is required for Osseoflex® SB placement. The Osseoflex® SB device does not create an access channel; the Osseoflex SB is designed to follow a pre-existing channel created by an access channel device. If the balloon has an Articulating Stylet inserted it enables the steerable feature of the balloon. The articulating or steering feature of the device assists the clinician in directing the device through the pre-existing channel. The Osseoflex® SB actuation knob can be turned clockwise to aid in directing the distal portion of the device. Turning the actuation knob counter-clockwise will relax the device and allow the device to be returned to its start position. The device should be manipulated only while under fluoroscopic observation with radiographic equipment that provides high quality images. | Osseoflex SB Straight Balloon (10ga/4ml) | OSSEON LLC | |
| 2 | B330OT02220 | OT-0222 | The Osseoflex® SB is designed for use in balloon kyphoplasty. The balloon serves The Osseoflex® SB is designed for use in balloon kyphoplasty. The balloon serves to create a cavity in the vertebral body, thereby reducing the fracture while still allowing for cement interdigitation. The balloon catheter is the functional part of the device that creates a cavity and reduces the fracture. The balloon catheter provides a conduit through which the physician can inflate the balloon at the distal end of the catheter. After the bone is disrupted, PMMA is injected through an Osseoflex® SN steerable needle to fill the previously created void(s).An access channel is required for Osseoflex® SB placement. The Osseoflex® SB device does not create an access channel; the Osseoflex® SB is designed to follow a pre-existing channel created by an access channel device. If the balloon has an Articulating Stylet inserted it enables the steerable feature of the balloon. The articulating or steering feature of the device assists the clinician in directing the device through the pre-existing channel. The Osseoflex® SB actuation knob can be turned clockwise to aid in directing the distal portion of the device. Turning the actuation knob counter-clockwise will relax the device and allow the device to be returned to its start position. The device should be manipulated only while under fluoroscopic observation with radiographic equipment that provides high quality images. | Osseoflex SB Straight Balloon (10ga/2ml) | OSSEON LLC | |
| 3 | B330OF82220 | OF-8222 | The Osseoflex® SB is designed for use in balloon kyphoplasty. The balloon serves The Osseoflex® SB is designed for use in balloon kyphoplasty. The balloon serves to create a cavity in the vertebral body, thereby reducing the fracture while still allowing for cement interdigitation. The balloon catheter is the functional part of the device that creates a cavity and reduces the fracture. The balloon catheter provides a conduit through which the physician can inflate the balloon at the distal end of the catheter. After the bone is disrupted, PMMA is injected through an Osseoflex® SN+ steerable needle to fill the previously created void(s).An access channel is required for Osseoflex® SB placement. The Osseoflex® SB device does not create an access channel; the Osseoflex® SB is designed to follow a pre-existing channel created by an access channel device. The articulating or steering feature of the device assists the clinician in directing the device through the pre-existingchannel. The Osseoflex® SB knob can be turned clockwise to aid in directing the distal portion of the device. Turning the knob counter-clockwise will relax the device and allow the device to be returned to its start position. The device should be manipulated only while under fluoroscopic observation with radiographic equipment that provides high quality images. | Osseoflex SB Steerable Balloon (8ga/2ml) | OSSEON LLC | |
| 4 | B330OF02240 | OF-0224 | The Osseoflex® SB is designed for use in balloon kyphoplasty. The balloon serves The Osseoflex® SB is designed for use in balloon kyphoplasty. The balloon serves to create a cavity in the vertebral body, thereby reducing the fracture while still allowing for cement interdigitation. The balloon catheter is the functional part of the device that creates a cavity and reduces the fracture. The balloon catheter provides a conduit through which the physician can inflate the balloon at the distal end of the catheter. After the bone is disrupted, PMMA is injected through an Osseoflex® SN steerable needle to fill the previously created void(s).An access channel is required for Osseoflex® SB placement. The Osseoflex® SB device does not create an access channel; the Osseoflex® SB is designed to follow a pre-existing channel created by an access channel device.If the balloon has an Articulating Stylet inserted it enables the steerable feature of the balloon. The articulating or steering feature of the device assists the clinician in directing the device through the pre-existing channel. The Osseoflex® SB actuation knob can be turned clockwise to aid in directing the distal portion of the device. Turning the actuation knob counter-clockwise will relax the device and allow the device to be returned to its start position. The device should be manipulated only while under fluoroscopic observation with radiographic equipment that provides high quality images. | Osseoflex SB Steerable Balloon ( 10 ga/ 4ml) | OSSEON LLC | |
| 5 | B330OF02220 | OF-0222 | The Osseoflex® SB is designed for use in balloon kyphoplasty. The balloon serves The Osseoflex® SB is designed for use in balloon kyphoplasty. The balloon serves to create a cavity in the vertebral body, thereby reducing the fracture while still while still allowing for cement interdigitation. The balloon catheter is the functional part of the device that creates a cavity and reduces the fracture. The balloon catheter provides a conduit through which the physician can inflate the balloon at the distal end of the catheter. After the bone is disrupted, PMMA is injected through an Osseoflex® SN steerable needle to fill the previously created void(s). An access channel is required for the Osseoflex® SB placement. The Osseoflex® SB device does not create an access channel; the Osseoflex® SB is designed to follow a pre-existing channel created by an access channel device.If the balloon has an Articulating Stylet inserted it enables the steerable feature of the balloon. The articulating or steering feature of the device assists the clinician in directing the device through the pre-existing channel. The Osseoflex® SB actuation knob can be turned clockwise to aid in directing the distal portion of the device. Turning the actuation knob counter-clockwise will relax the device and allow the device to be returned to it's start position. The device should be manipulated only while under fluoroscopic observation with radiographic equipment that provides high quality images. | Osseoflex SB Steerable Balloon (10ga/2ml) | OSSEON LLC | |
| 6 | B330OF00050 | OF-0005 | The Osseoflex® SB is designed for use in balloon kyphoplasty. The balloon serves The Osseoflex® SB is designed for use in balloon kyphoplasty. The balloon serves to create a cavity in the vertebral body, thereby reducing the fracture while still allowing for cement interdigitation. The balloon catheter is the functional part of the device that creates a cavity and reduces the fracture. The balloon catheter provides a conduit through which the physician can inflate the balloon at the distal end of the catheter. After the bone is disrupted, PMMA is injected through an Osseoflex® SN+ steerable needle to fill the previously created void(s).An access channel is required for Osseoflex® SB placement. The Osseoflex® SB device does not create an access channel; the Osseoflex® SB is designed to follow a pre-existing channel created by an access channel device. The articulating or steering feature of the device assists the clinician in directing the device through the pre-existingchannel. The Osseoflex® SB knob can be turned clockwise to aid in directing the distal portion of the device. Turning the knob counter-clockwise will relax the device and allow the device to be returned to its start position. The device should be manipulated only while under fluoroscopic observation with radiographic equipment that provides high quality images. | Osseoflex SB Steerable Balloon (8ga/ 4ml) | OSSEON LLC | |
| 7 | 30808232000949 | 2110-0031 | 2110-0031 | Mix Tips, Luer | Cortoss | STRYKER CORPORATION |
| 8 | 28031497001382 | 13C2040 | Mendec Spine HV System is indicated for the treatment of pathological fractures Mendec Spine HV System is indicated for the treatment of pathological fractures of the vertebral body using a vertebroplasty or kyphoplasty procedure.Mendec Spine HV System is a closed sysyem which containes the powder and liquid components separately.The device is disposable and sterile. | Mendec Spine HV System | TECRES SPA | |
| 9 | 28031497000521 | 13C2000 | Mendec Spine Kit is a device for the treatment of pathological fractures of the Mendec Spine Kit is a device for the treatment of pathological fractures of the vertebral body using a vertebroplasty procedure.The device is composed by an acrylic resin and a delivery system. | Mendec Spine Kit | TECRES SPA | |
| 10 | 28031497000101 | 1230 | Mendec Spine is an acrylic resin for the treatment of pathological fractures of Mendec Spine is an acrylic resin for the treatment of pathological fractures of the vertebral body using a vertebroplasty or kyphoplasty procedure.Mendec Spine is a medium-high viscosity acrylic resin (PMMA-based), highly radiopaque for syringe application.The device is sold disposable and sterile | Mendec Spine | TECRES SPA | |
| 11 | 15056033810538 | INTV-CEM | Osteoflex | PAN MEDICAL US CORPORATION | ||
| 12 | 10885403242021 | VBT1110 | VBT1110 | AVAMAX™ VERTEBRAL BALLOON TRAY 11GX10MM | AVAmax | CAREFUSION 2200, INC |
| 13 | 10885403241192 | AFB1130 | AFB1130 | AVAFLEX™ VERTEBRAL BALLOON SYSTEM 11GX30MM | AVAflex | CAREFUSION 2200, INC |
| 14 | 10885403241185 | AFB1120 | AFB1120 | AVAFLEX™ VERTEBRAL BALLOON SYSTEM 11GX20MM | AVAflex | CAREFUSION 2200, INC |
| 15 | 10885403241178 | AFB1115 | AFB1115 | AVAFLEX™ VERTEBRAL BALLOON SYSTEM 11GX15MM | AVAflex | CAREFUSION 2200, INC |
| 16 | 10885403240911 | VBT1320 | VBT1320 | AVAMAX™ VERTEBRAL BALLOON TRAY 13GX20MM | AVAmax | CAREFUSION 2200, INC |
| 17 | 10885403240904 | VBT1315 | VBT1315 | AVAMAX™ VERTEBRAL BALLOON TRAY 13GX15MM | AVAmax | CAREFUSION 2200, INC |
| 18 | 10885403240898 | VBT1310 | VBT1310 | AVAMAX™ VERTEBRAL BALLOON TRAY 13GX10MM | AVAmax | CAREFUSION 2200, INC |
| 19 | 10885403225796 | AFB1030 | AFB1030 | AVAFLEX™ VERTEBRAL BALLOON SYSTEM 10GX20MM | AVAflex | CAREFUSION 2200, INC |
| 20 | 10885403223259 | AFB1015 | AFB1015 | AVAFLEX™ VERTEBRAL BALLOON SYSTEM 10GX15MM | AVAflex | CAREFUSION 2200, INC |
| 21 | 10885403223242 | AFB1020 | AFB1020 | AVAFLEX™ VERTEBRAL BALLOON SYSTEM 10GX20MM | AVAflex | CAREFUSION 2200, INC |
| 22 | 10885403176593 | VBT1120 | VBT1120 | AVAMAX™ VERTEBRAL BALLOON TRAY 11GX20MM | AVAmax | CAREFUSION 2200, INC |
| 23 | 10885403176586 | VBT1115 | VBT1115 | AVAMAX™ VERTEBRAL BALLOON TRAY 11GX15MM | AVAmax | CAREFUSION 2200, INC |
| 24 | 10885403120022 | VBT1015 | VBT1015 | AVAMAX™ VERTEBRAL BALLOON TRAY 10GX15MM | AVAmax | CAREFUSION 2200, INC |
| 25 | 10885403119996 | VBT1010 | VBT1010 | AVAMAX™ VERTEBRAL BALLOON TRAY 10GX10MM | AVAmax | CAREFUSION 2200, INC |
| 26 | 10885403119804 | VBT1020 | VBT1020 | AVAMAX™ VERTEBRAL BALLOON TRAY 10GX20MM | AVAmax | CAREFUSION 2200, INC |
| 27 | 10885403002120 | VMXXLCT | VMXXLCT | AVAmax PLUS Extra Level Tray Bone Cement Delivery System | AVAmax | CAREFUSION 2200, INC |
| 28 | 10885403002113 | VMX00CT | VMX00CT | AVAmax PLUS Bone Cement Delivery System | AVAmax | CAREFUSION 2200, INC |
| 29 | 10885403002106 | BCTXLCT | BCTXLCT | AVAmax Extra Level Tray, Bone Cement Delivery System | AVAmax | CAREFUSION 2200, INC |
| 30 | 10885403002090 | BCT00CT | BCT00CT | AVAmax Bone Cement Delivery System | AVAmax | CAREFUSION 2200, INC |
| 31 | 10885403002069 | BCPM003 | BCPM003 | AVAtex Radiopaque Bone Cement | AVAtex | CAREFUSION 2200, INC |
| 32 | 10885403001932 | VBT0820 | VBT0820 | AVAMAX™ VERTEBRAL BALLOON TRAY 8GX20MM | AVAmax | CAREFUSION 2200, INC |
| 33 | 10885403001925 | VBT0815 | VBT0815 | AVAMAX™ VERTEBRAL BALLOON TRAY 8GX15MM | AVAmax | CAREFUSION 2200, INC |
| 34 | 10885403001918 | VBT0810 | VBT0810 | AVAMAX™ VERTEBRAL BALLOON TRAY 8GX10MM | AVAmax | CAREFUSION 2200, INC |
| 35 | 10827002432007 | G43200 | CVAK-100 | Vertebroplasty Ancillary Kit | Cook | COOK INCORPORATED |
| 36 | 10705034722726 | 03.804.702S | 03804702S | SYNFLATE BALLOON/LARGE- STERILE | SYNFLATE | SYNTHES GMBH |
| 37 | 10705034722719 | 03.804.701S | 03804701S | SYNFLATE BALLOON/MEDIUM- STERILE | SYNFLATE | SYNTHES GMBH |
| 38 | 10705034722702 | 03.804.700S | 03804700S | SYNFLATE BALLOON/SMALL- STERILE | SYNFLATE | SYNTHES GMBH |
| 39 | 10705034722627 | 03.804.502S | 03804502S | VERTEBRAL BODY BALLOON/LARGE- STERILE | VBB | SYNTHES GMBH |
| 40 | 10705034722610 | 03.804.501S | 03804501S | VERTEBRAL BODY BALLOON/MEDIUM- STERILE | VBB | SYNTHES GMBH |
| 41 | 10705034722603 | 03.804.500S | 03804500S | VERTEBRAL BODY BALLOON/SMALL- STERILE | VBB | SYNTHES GMBH |
| 42 | 10705034722597 | 03.804.413S | 03804413S | INFLATION SYSTEM-STERILE | NA | SYNTHES (U.S.A.) LP |
| 43 | 10705034209630 | 283913000 | 283913000 | CONFIDENCE SPINAL CEMENT SYSTEM CONFIDENCE KIT SPINAL CEMENT SYSTEM | CONFIDENCE SPINAL CEMENT SYSTEM | MEDOS INTERNATIONAL SÀRL |
| 44 | 10705034209623 | 283910000 | 283910000 | CONFIDENCE SPINAL CEMENT SYSTEM CONFIDENCE PLUS KIT SPINAL CEMENT SYSTEM 11cc | CONFIDENCE SPINAL CEMENT SYSTEM | MEDOS INTERNATIONAL SÀRL |
| 45 | 10705034209555 | 283905000 | 283905000 | CONFIDENCE SPINAL CEMENT SYSTEM CONFIDENCE KIT SPINAL CEMENT SYSTEM 5cc | CONFIDENCE SPINAL CEMENT SYSTEM | MEDOS INTERNATIONAL SÀRL |
| 46 | 08809695630231 | GSMD-00 | GSMD-00 | Tracker Plus Kyphoplasty System | GS MEDICAL CO., LTD. | |
| 47 | 08809695619939 | GVCD-1000 | GVCD-1000 | Tracker Plus Kyphoplasty System | GS MEDICAL CO., LTD. | |
| 48 | 08809695619861 | GCD-FD1100 | GCD-FD1100 | Tracker Plus Kyphoplasty System | GS MEDICAL CO., LTD. | |
| 49 | 08809695619830 | GSCK-01 | GSCK-01 | Tracker Plus Kyphoplasty System | GS MEDICAL CO., LTD. | |
| 50 | 08809695619748 | GSDK-01 | GSDK-01 | Tracker Plus Kyphoplasty System | GS MEDICAL CO., LTD. |