| No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
|---|---|---|---|---|---|---|---|---|
| 1 | 00885825020781 | N/A | 394.89 | Carbon Fiber Rod | KTT | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT | 2 | N/A |
| 2 | 00885825020774 | N/A | 394.88 | Carbon Fiber Rod | KTT | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT | 2 | N/A |
| 3 | 00885825020767 | N/A | 394.80 | Carbon Fiber Rod | KTT | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT | 2 | N/A |
| 4 | 00885825020750 | N/A | 395.782 | Carbon Fiber Rod | KTT | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT | 2 | N/A |
| 5 | 00885825020743 | N/A | 395.784 | Carbon Fiber Rod | KTT | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT | 2 | N/A |
| 6 | 00885825020736 | N/A | 394.87 | Carbon Fiber Rod | KTT | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT | 2 | N/A |
| 7 | 00885825020729 | N/A | 394.82 | Carbon Fiber Rod | KTT | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT | 2 | N/A |
| 8 | 00885825020712 | N/A | 394.83 | Carbon Fiber Rod | KTT | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT | 2 | N/A |
| 9 | 00885825020705 | N/A | 394.84 | Carbon Fiber Rod | KTT | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT | 2 | N/A |
| 10 | 00885825020699 | N/A | 394.86 | Carbon Fiber Rod | KTT | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT | 2 | N/A |
| 11 | 00885825020682 | N/A | 394.85 | Carbon Fiber Rod | KTT | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT | 2 | N/A |
| 12 | 00885825020590 | N/A | 390.007 | Tube to Tube Clamp | KTT | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT | 2 | N/A |
| 13 | 00885825020583 | N/A | 390.004 | Multi-Pin Clamp | KTT | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT | 2 | N/A |
| 14 | 00885825020576 | N/A | 390.003 | Rod Attachment | KTT | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT | 2 | N/A |
| 15 | 00885825020569 | N/A | 390.002 | Multi-Pin Clamp | KTT | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT | 2 | N/A |
| 16 | 00885825020361 | N/A | 4455-55-11RP | Universal Clamp | KTT | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT | 2 | N/A |
| 17 | 00885825020354 | N/A | 4455-15-11RP | Universal Clamp | KTT | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT | 2 | N/A |
| 18 | 00885825020347 | N/A | 4452-55-11RP | Universal Clamp | KTT | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT | 2 | N/A |
| 19 | 00885825020330 | N/A | 4452-25-51RP | Rod to Rod Clamp | KTT | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT | 2 | N/A |
| 20 | 00885825020323 | N/A | 4452-25-28RP | Rod to Rod Clamp | KTT | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT | 2 | N/A |
| 21 | 00885825020316 | N/A | 4452-15-81RP | Rod to Rod Clamp | KTT | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT | 2 | N/A |
| 22 | 00885825020309 | N/A | 4452-15-48RP | Rod to Rod Clamp | KTT | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT | 2 | N/A |
| 23 | 00885825020293 | N/A | 4452-15-11RP | Rod to Rod Clamp | KTT | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT | 2 | N/A |
| 24 | 00885825020286 | N/A | 4451-08-30RP | Carbon Fiber Rod | KTT | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT | 2 | N/A |
| 25 | 00885825020279 | N/A | 4451-08-16RP | Carbon Fiber Rod | KTT | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT | 2 | N/A |
| 26 | 00885825020262 | N/A | 4451-08-12RP | Carbon Fiber Rod | KTT | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT | 2 | N/A |
| 27 | 00885825020255 | N/A | 4451-08-10RP | Carbon Fiber Rod | KTT | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT | 2 | N/A |
| 28 | 00885825020248 | N/A | 4451-01-55RP | Carbon Fiber Rod | KTT | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT | 2 | N/A |
| 29 | 00885825020231 | N/A | 4451-01-50RP | Carbon Fiber Rod | KTT | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT | 2 | N/A |
| 30 | 00885825020224 | N/A | 4451-01-45RP | Carbon Fiber Rod | KTT | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT | 2 | N/A |
| 31 | 00885825020217 | N/A | 4451-01-40RP | Carbon Fiber Rod | KTT | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT | 2 | N/A |
| 32 | 00885825020200 | N/A | 4451-01-35RP | Carbon Fiber Rod | KTT | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT | 2 | N/A |
| 33 | 00885825020194 | N/A | 4451-01-30RP | Carbon Fiber Rod | KTT | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT | 2 | N/A |
| 34 | 00885825020187 | N/A | 4451-01-25RP | Carbon Fiber Rod | KTT | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT | 2 | N/A |
| 35 | 00885825020170 | N/A | 4451-01-20RP | Carbon Fiber Rod | KTT | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT | 2 | N/A |
| 36 | 00885825020163 | N/A | 4451-01-15RP | Carbon Fiber Rod | KTT | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT | 2 | N/A |
| 37 | 00885825020156 | N/A | 4451-01-12RP | Carbon Fiber Rod | KTT | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT | 2 | N/A |
| 38 | 00885825020149 | N/A | 4451-01-10RP | Carbon Fiber Rod | KTT | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT | 2 | N/A |
| 39 | 00885825020132 | N/A | 395.796RP | Carbon Fiber Rod | KTT | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT | 2 | N/A |
| 40 | 00885825020125 | N/A | 395.792RP | Carbon Fiber Rod | KTT | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT | 2 | N/A |
| 41 | 00885825020118 | N/A | 395.788RP | Carbon Fiber Rod | KTT | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT | 2 | N/A |
| 42 | 00885825020101 | N/A | 395.786RP | Carbon Fiber Rod | KTT | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT | 2 | N/A |
| 43 | 00885825020095 | N/A | 395.784RP | Carbon Fiber Rod | KTT | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT | 2 | N/A |
| 44 | 00885825020088 | N/A | 395.782RP | Carbon Fiber Rod | KTT | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT | 2 | N/A |
| 45 | 00885825020071 | N/A | 395.780RP | Ex Fix Component | KTT | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT | 2 | N/A |
| 46 | 00885825020064 | N/A | 395.779RP | Carbon Fiber Rod | KTT | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT | 2 | N/A |
| 47 | 00885825020675 | N/A | 5150-3-065 | MonoTube Triax Pin Clamp External Fixation System | KTT | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT | 2 | N/A |
| 48 | 00885825020668 | N/A | 393.64 | Adjustable Clamp | KTT | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT | 2 | N/A |
| 49 | 00885825020651 | N/A | 390.012 | 30 Degress Outrigger Post | KTT | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT | 2 | N/A |
| 50 | 00885825020910 | N/A | 10438577 | Diagnostic Ultrasound Catheter, 10F | OWQ | Reprocessed intravascular ultrasound catheter | 2 | N/A |
| No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
|---|---|---|---|---|---|---|
| 1 | B39034191 | 3419 | Reprocessed 2.9mm Full Radius Blade | SURETEK MEDICAL | ||
| 2 | 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 | |
| 3 | 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 | |
| 4 | 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 | |
| 5 | 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 | |
| 6 | 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 | |
| 7 | 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 | |
| 8 | B235MDK00010 | MDK-0001 | MDK-0001 | mild Device Kit | VERTOS MEDICAL, INC. | |
| 9 | B192300311000 | 30-0311-00 | 30-0311-00 | 4.0 mm, 45 deg. Sinuscope, l=175mm, autoclavable | IEC-Innoview GmbH | INNOVATIVE ENDOSCOPY COMPONENTS, L.L.C. |
| 10 | B192300012000 | 30-0012-00 | 30-0012-00 | 4.0 mm, 70 deg. Arthroscope, l=175mm, autoclavable | IEC-Innoview GmbH | INNOVATIVE ENDOSCOPY COMPONENTS, L.L.C. |
| 11 | B192300011000 | 30-0011-00 | 30-0011-00 | 4.0 mm, 30 deg. Arthroscope, l=175mm, autoclavable | IEC-Innoview GmbH | INNOVATIVE ENDOSCOPY COMPONENTS, L.L.C. |
| 12 | B192300010000 | 30-0010-00 | 30-0010-00 | 4.0 mm, 0 deg. Arthroscope, l=175mm, autoclavable | IEC-Innoview GmbH | INNOVATIVE ENDOSCOPY COMPONENTS, L.L.C. |
| 13 | B192300008000 | 30-0008-00 | 30-0008-00 | 2.7 mm, 30 deg. Arthroscope, l=187.5mm, autoclavable | IEC-Innoview GmbH | INNOVATIVE ENDOSCOPY COMPONENTS, L.L.C. |
| 14 | B192300006000 | 30-0006-00 | 30-0006-00 | 2.7 mm, 70 deg. Arthroscope, l=175mm, autoclavable | IEC-Innoview GmbH | INNOVATIVE ENDOSCOPY COMPONENTS, L.L.C. |
| 15 | B192300004000 | 30-0004-00 | 30-0004-00 | 2.7 mm, 0 deg. Arthroscope, l=175mm, autoclavable | IEC-Innoview GmbH | INNOVATIVE ENDOSCOPY COMPONENTS, L.L.C. |
| 16 | B192300003000 | 30-0003-00 | 30-0003-00 | 2.7 mm, 70 deg. Arthroscope, l=110mm, autoclavable | IEC-Innoview GmbH | INNOVATIVE ENDOSCOPY COMPONENTS, L.L.C. |
| 17 | B089B659660 | B65966 | B65966 | ENDOPLASTIC SCOPE; 12''(33CM, )30 DEGREE, 10MM DIAMETER, | ENDOPLASTIC SCOPE | BLACK & BLACK SURGICAL, INC. |
| 18 | B089B659320 | B65932 | B65932 | SINUSCOPE OBTURATOR CONICAL BLUNT, 3.0 MM, 140 LENGTH | N/A | BLACK & BLACK SURGICAL, INC. |
| 19 | B089B659310 | B65931 | B65931 | SINUSCOPE TROCAR WITH PYRAMIDAL TIP, 3.0 MM, 140 LENGTH | N/A | BLACK & BLACK SURGICAL, INC. |
| 20 | B089B659300 | B65930 | B65930 | SINUSCOPE TROCAR SLEEVE, UNIVERSAL, FOR 3.0 MM SCOPES, 140 LENGTH, "0"d, "30"d, "70"d | N/A | BLACK & BLACK SURGICAL, INC. |
| 21 | B089B659250 | B65925 | B65925 | ENDOPLASTIC SCOPE; 12''(33CM), 0 DEGREE, 10MM DIAMETER | ENDOPLASTIC SCOPE | BLACK & BLACK SURGICAL, INC. |
| 22 | B089B659220 | B65922 | B65922 | ENDOPLASTIC SCOPE; 7"(18CM), 0 DEGREE, 4MM DIAMETER | ENDOPLASTIC SCOPE | BLACK & BLACK SURGICAL, INC. |
| 23 | B089B659210 | B65921 | B65921 | ENDOPLASTIC SCOPE; 7''(17.5CM), 30 DEGREE, 4MM DIAMETER, | ENDOPLASTIC SCOPE | BLACK & BLACK SURGICAL, INC. |
| 24 | B089B659200 | B65920 | B65920 | ENDOPLASTIC SCOPE; 7"(17.5CM), 30 DEGREE, 5MM DIAMETER | ENDOPLASTIC SCOPE | BLACK & BLACK SURGICAL, INC. |
| 25 | B089B659100 | B65910 | B65910 | ENDOPLASTIC SCOPE; 7''(17.5CM), 30 DEGREE, 10MM DIAMETER | ENDOPLASTIC SCOPE | BLACK & BLACK SURGICAL, INC. |
| 26 | B089B659050 | B65905 | B65905 | OTOSCOPE; 1.6''(41MM), 0 DEGREE, 2.7MM DIAMETER, AUTOCLAVABLE | N/A | BLACK & BLACK SURGICAL, INC. |
| 27 | B089B659010 | B65901 | B65901 | SINUSCOPE; 5 3/4"(14.0CM), "30" DEGREE, 3.0MM DIAMETER, AUTOCLAVABLE | N/A | BLACK & BLACK SURGICAL, INC. |
| 28 | B089B659000 | B65900 | B65900 | SINUSCOPE; 5 3/4"(14.0CM), "0" DEGREE, 3.0MM DIAMETER, AUTOCLAVABLE | N/A | BLACK & BLACK SURGICAL, INC. |
| 29 | B067212001 | 21200 | 21200 | 2.0 MM Short Kit with aspiration bottle | Nucleotome | CLARUS MEDICAL, LLC |
| 30 | 30845854648517 | CV4040 | CV4040 | CrystalView™ Pro Autoclavable Remote Control | CrystalView | CONMED CORPORATION |
| 31 | 30845854648500 | CV4000 | CV4000 | CrystalView™ Pro Irrigation Console | CRYSTALVIEW | CONMED CORPORATION |
| 32 | 30845854083424 | UHD4700CM | UHD4700CM | 4.0mm, 70° UHD Quicklatch C-Mount Arthroscope, 157 mm WL | NA | CONMED CORPORATION |
| 33 | 30845854083417 | UHD4300CM | UHD4300CM | 4.0mm, 30° UHD Quicklatch C-Mount Arthroscope, 157 mm WL | NA | CONMED CORPORATION |
| 34 | 30845854083400 | UHD4000CM | UHD4000CM | 4.0mm, 0° UHD Quicklatch C-Mount Arthroscope, 157 mm WL | NA | CONMED CORPORATION |
| 35 | 30845854041127 | E9000 | E9000 | E9000 CONTROLLER 115 VAC | NA | CONMED CORPORATION |
| 36 | 30845854040533 | E9005RFB | E9005RFB | RFB, E9000 HIGH SPEED SHAVER | NA | CONMED CORPORATION |
| 37 | 30845854037816 | 25.1007 | 25.1007 | 4MM STRAIGHT RASP, OSTEOPREP | NA | CONMED CORPORATION |
| 38 | 30845854037809 | 25.1005 | 25.1005 | 4MM OPEN CURETTE, OSTEOPREP | NA | CONMED CORPORATION |
| 39 | 30845854035553 | E9015 | E9015 | E9000 CRANIAL PERFORATOR DRIVE | E9000 | CONMED CORPORATION |
| 40 | 30845854035546 | E9011-9 | E9011-9 | E9000 LONG NEURO GUARD | NA | CONMED CORPORATION |
| 41 | 30845854035539 | E9011-8 | E9011-8 | E9000 MEDIUM NEURO GUARD | NA | CONMED CORPORATION |
| 42 | 30845854035522 | E9011-3 | E9011-3 | E9000, EXTRA-LONG BUR GUARD | NA | CONMED CORPORATION |
| 43 | 30845854035515 | E9011-2 | E9011-2 | E9000 LONG BUR GUARD | NA | CONMED CORPORATION |
| 44 | 30845854035508 | E9011-1 | E9011-1 | E9000 MEDIUM BUR GUARD | NA | CONMED CORPORATION |
| 45 | 30845854035492 | E9010 | E9010 | COOLFLEX E9000 HIGH SPEED DRILL | NA | CONMED CORPORATION |
| 46 | 30845854035485 | E9005 | E9005 | E9000 HIGH SPEED SHAVER | NA | CONMED CORPORATION |
| 47 | 30845854027039 | E9011-7 | E9011-7 | E9000 SHORT NEURO GUARD | NA | CONMED CORPORATION |
| 48 | 30845854024458 | 25.1006 | 25.1006 | 4MM CUPPED CURETTE, OSTEOPREP | NA | CONMED CORPORATION |
| 49 | 30845854012110 | E9000G | E9000G | E9000G CONTROLLER 230 VAC | NA | CONMED CORPORATION |
| 50 | 30653405987509 | CV4000 | CV4000 | CrystalView™ Pro Irrigation Console | CRYSTALVIEW | CONMED CORPORATION |