Other products from "COOK INCORPORATED"
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 00827002473096 G47309 N5.0-35-100-P-10S-0-CSC-20-01 Centimeter Sizing Catheter DQO CATHETER, INTRAVASCULAR, DIAGNOSTIC 2 Cook
2 00827002473089 G47308 N5.0-35-100-P-10S-PIG-CSC-20-01 Centimeter Sizing Catheter DQO CATHETER, INTRAVASCULAR, DIAGNOSTIC 2 Cook
3 00827002472990 G47299 N5.0-35-90-P-10S-PIG-WSC-MCVA-100893-01 White Sizing Catheter DQO CATHETER, INTRAVASCULAR, DIAGNOSTIC 2 Cook
4 00827002472983 G47298 N5.0-35-70-P-10S-PIG-WSC-01 White Sizing Catheter DQO CATHETER, INTRAVASCULAR, DIAGNOSTIC 2 Cook
5 00827002479302 G47930 IMWCE-38-4-7 MReye Embolization Coil KRD Device, Vascular, for Promoting Embolization 2 MReye
6 00827002479296 G47929 IMWCE-38-4-12 MReye Embolization Coil KRD Device, Vascular, for Promoting Embolization 2 MReye
7 00827002479289 G47928 IMWCE-38-4-10 MReye Embolization Coil KRD Device, Vascular, for Promoting Embolization 2 MReye
8 00827002479272 G47927 IMWCE-38-4-8 MReye Embolization Coil KRD Device, Vascular, for Promoting Embolization 2 MReye
9 00827002479265 G47926 IMWCE-38-3-2 MReye Embolization Coil KRD Device, Vascular, for Promoting Embolization 2 MReye
10 00827002479258 G47925 IMWCE-38-2-8 MReye Embolization Coil KRD Device, Vascular, for Promoting Embolization 2 MReye
11 00827002424364 G42436 IMWCE-35-10-4 MReye Embolization Coil KRD Device, Vascular, for Promoting Embolization 2 MReye
12 00827002479241 G47924 IMWCE-38-2-6 MReye Embolization Coil KRD Device, Vascular, for Promoting Embolization 2 MReye
13 00827002479234 G47923 IMWCE-38-2-5 MReye Embolization Coil KRD Device, Vascular, for Promoting Embolization 2 MReye
14 00827002479227 G47922 IMWCE-38-2-4 MReye Embolization Coil KRD Device, Vascular, for Promoting Embolization 2 MReye
15 00827002479210 G47921 IMWCE-38-2-2 MReye Embolization Coil KRD Device, Vascular, for Promoting Embolization 2 MReye
16 00827002479203 G47920 IMWCE-38-15-2 MReye Embolization Coil KRD Device, Vascular, for Promoting Embolization 2 MReye
17 00827002479197 G47919 IMWCE-38-13-8 MReye Embolization Coil KRD Device, Vascular, for Promoting Embolization 2 MReye
18 00827002479180 G47918 IMWCE-38-12-5 MReye Embolization Coil KRD Device, Vascular, for Promoting Embolization 2 MReye
19 00827002478923 G47892 IMWCE-35-14-5 MReye Embolization Coil KRD Device, Vascular, for Promoting Embolization 2 MReye
20 00827002478916 G47891 IMWCE-35-14-3 MReye Embolization Coil KRD Device, Vascular, for Promoting Embolization 2 MReye
21 00827002424272 G42427 IMWCE-35-6-5 MReye Embolization Coil KRD Device, Vascular, for Promoting Embolization 2 MReye
22 00827002424234 G42423 IMWCE-35-5-8 MReye Embolization Coil KRD Device, Vascular, for Promoting Embolization 2 MReye
23 00827002424197 G42419 IMWCE-35-5-3 MReye Embolization Coil KRD Device, Vascular, for Promoting Embolization 2 MReye
24 00827002424180 G42418 IMWCE-35-4-8 MReye Embolization Coil KRD Device, Vascular, for Promoting Embolization 2 MReye
25 00827002424173 G42417 IMWCE-35-4-6 MReye Embolization Coil KRD Device, Vascular, for Promoting Embolization 2 MReye
26 00827002424142 G42414 IMWCE-35-4-3 MReye Embolization Coil KRD Device, Vascular, for Promoting Embolization 2 MReye
27 00827002424111 G42411 IMWCE-35-3-6 MReye Embolization Coil KRD Device, Vascular, for Promoting Embolization 2 MReye
28 00827002424104 G42410 IMWCE-35-3-5 MReye Embolization Coil KRD Device, Vascular, for Promoting Embolization 2 MReye
29 00827002424098 G42409 IMWCE-35-3-4 MReye Embolization Coil KRD Device, Vascular, for Promoting Embolization 2 MReye
30 00827002424081 G42408 IMWCE-35-3-3 MReye Embolization Coil KRD Device, Vascular, for Promoting Embolization 2 MReye
31 00827002424074 G42407 IMWCE-35-2-4 MReye Embolization Coil KRD Device, Vascular, for Promoting Embolization 2 MReye
32 00827002424067 G42406 IMWCE-35-2-3 MReye Embolization Coil KRD Device, Vascular, for Promoting Embolization 2 MReye
33 00827002424043 G42404 IMWCE-35-1-5 MReye Embolization Coil KRD Device, Vascular, for Promoting Embolization 2 MReye
34 00827002141377 G14137 072010 Fascial Dilator KOE DILATOR, URETHRAL 2 Cook
35 00827002424029 G42402 IMWCE-25-5-8 MReye Embolization Coil KRD Device, Vascular, for Promoting Embolization 2 MReye
36 00827002423978 G42397 IMWCE-25-3-2 MReye Embolization Coil KRD Device, Vascular, for Promoting Embolization 2 MReye
37 00827002166998 G16699 083310 Cook Cystostomy Catheter Set KOB CATHETER, SUPRAPUBIC (AND ACCESSORIES) 2 Cook
38 00827002142794 G14279 073732 Fascial Dilator KOE DILATOR, URETHRAL 2 Cook
39 00827002142787 G14278 073730 Fascial Dilator KOE DILATOR, URETHRAL 2 Cook
40 00827002142763 G14276 073726 Fascial Dilator KOE DILATOR, URETHRAL 2 Cook
41 00827002141896 G14189 073714 Fascial Dilator KOE DILATOR, URETHRAL 2 Cook
42 00827002589865 G58986 ESLMY-5.0-32J-1-15 Cook CVC Single Lumen Central Venous Catheter Set FOZ Catheter, intravascular, therapeutic, short-term less than 30 days 2 Cook
43 00827002589858 G58985 ESLM-6.3-32J-1-15 Cook CVC Single Lumen Central Venous Catheter Set FOZ Catheter, intravascular, therapeutic, short-term less than 30 days 2 Cook
44 00827002589841 G58984 ESLM-5.0-32J-1-15 Cook CVC Single Lumen Central Venous Catheter Set FOZ Catheter, intravascular, therapeutic, short-term less than 30 days 2 Cook
45 00827002589834 G58983 ESLM-5.0-32J-0-15 Cook CVC Single Lumen Central Venous Catheter Set FOZ Catheter, intravascular, therapeutic, short-term less than 30 days 2 Cook
46 00827002589827 G58982 UTLMY-9.0-32J-1-20-IHI Cook CVC Triple Lumen Power-Injectable Central Venous Catheter Set FOZ Catheter, intravascular, therapeutic, short-term less than 30 days 2 Cook
47 00827002589810 G58981 UTLMY-9.0-32J-1-20 Cook CVC Triple Lumen Power-Injectable Central Venous Catheter Set FOZ Catheter, intravascular, therapeutic, short-term less than 30 days 2 Cook
48 00827002589803 G58980 UTLMY-9.0-32J-1-25-IHI Cook CVC Triple Lumen Power-Injectable Central Venous Catheter Set FOZ Catheter, intravascular, therapeutic, short-term less than 30 days 2 Cook
49 00827002589797 G58979 UTLMY-9.0-32J-1-25 Cook CVC Triple Lumen Power-Injectable Central Venous Catheter Set FOZ Catheter, intravascular, therapeutic, short-term less than 30 days 2 Cook
50 00827002589780 G58978 UTLMY-9.0-32J-1-15-IHI Cook CVC Triple Lumen Power-Injectable Central Venous Catheter Set FOZ Catheter, intravascular, therapeutic, short-term less than 30 days 2 Cook
Other products with the same Product Code "NDN"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 00690521015388 15-814 15-814 Padlock Security Tags Batrik Red Padlock Security Tags BATRIK MEDICAL MANUFACTURING INC
2 00643169097865 C01A BONE CEMENT C01A HV-R US KYPHON® HV-R® Bone Cement MEDTRONIC SOFAMOR DANEK, INC.
3 00643169097834 C01B BONE CEMENT C01B HV-R WITH MIXER US KYPHON® HV-R® Bone Cement and KYPHON® Mixer Pack MEDTRONIC SOFAMOR DANEK, INC.
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5 00643169097803 CX01A BONE CEMENT CX01A XPEDE US KYPHON® Xpede™ Bone Cement MEDTRONIC SOFAMOR DANEK, INC.
6 00643169097797 CX01B BONE CEMENT CX01B XPEDE W MIXER US KYPHON® Xpede™ Bone Cement and KYPHON® Mixer Pack MEDTRONIC SOFAMOR DANEK, INC.
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8 00613994746931 C10A BONE CEMENT C10A KYPHON ACTIVOS 10 ActivOs™ 10 Bone Cement MEDTRONIC SOFAMOR DANEK, INC.
9 00613994745606 C01A BONE CEMENT C01A HV-R CAN KYPHON® HV-R® Bone Cement MEDTRONIC SOFAMOR DANEK, INC.
10 00613994745590 C01A BONE CEMENT C01A HV-R US KYPHON® HV-R® Bone Cement MEDTRONIC SOFAMOR DANEK, INC.
11 00613994745569 C01B BONE CEMENT C01B HV-R WITH MIXER CAN KYPHON® HV-R® Bone Cement and KYPHON® Mixer Pack MEDTRONIC SOFAMOR DANEK, INC.
12 00613994745552 C01B BONE CEMENT C01B HV-R WITH MIXER US KYPHON® HV-R® Bone Cement and KYPHON® Mixer Pack MEDTRONIC SOFAMOR DANEK, INC.
13 00613994583215 C01A CEMENT C01A KYPHX HV-R BONE CEMENT EN KYPHON® HV-R® Bone Cement MEDTRONIC SOFAMOR DANEK, INC.
14 00613994515155 C01B BONE CEMENT C01B HV-R WITH MIXER US KYPHON® HV-R® Bone Cement and KYPHON® Mixer Pack MEDTRONIC SOFAMOR DANEK, INC.
15 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
16 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
17 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
18 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
19 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
20 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
21 30808232000949 2110-0031 2110-0031 Mix Tips, Luer Cortoss STRYKER CORPORATION
22 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
23 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
24 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
25 15056033810538 INTV-CEM Osteoflex PAN MEDICAL US CORPORATION
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49 10827002432007 G43200 CVAK-100 Vertebroplasty Ancillary Kit Cook COOK INCORPORATED
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