| No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
|---|---|---|---|---|---|---|---|---|
| 1 | 00858439001675 | 9210854 | PosiSep C 0.6 x 2.0 devices are patient-comfortable sponges manufactured from na PosiSep C 0.6 x 2.0 devices are patient-comfortable sponges manufactured from naturally occurring Chitosan polymers. PosiSep C 0.6 x 2.0 devices were specifically engineered for use as a nasal dressing to be used following clinic based procedures. | LYA,EMX | Splint, Intranasal Septal,Balloon, Epistaxis | 1 | PosiSep C 0.6 x 2.0 | |
| 2 | 00858439001774 | 9770013 | The kit includes the aerosol evacuator that has a white suction connector attach The kit includes the aerosol evacuator that has a white suction connector attached to tubing that terminates in a beveled end. Inserted on this tubing is a yellow foam seal and a black positioning ring that can both slide along the tubing. A spare larger foam seal and a male connector are also supplied. When surgery is performed in one nasal cavity, the AeroClear is placed in the contralateral cavity and connected to facility suction. | JOL | Catheter And Tip, Suction | AeroClear | ||
| 3 | 00858439001637 | 9110534 | NexPak X Intranasal Splint is a sterile flexible foam pad comprised of a lyophil NexPak X Intranasal Splint is a sterile flexible foam pad comprised of a lyophilized mixture of starch polysaccharide and polysaccharide binders. NexPak X Intranasal Splint is intended to minimize bleeding and edema and to prevent adhesions between the septum and nasal cavity. The intranasal splint is placed in the nasal cavity after surgery or trauma. | LYA | Splint, Intranasal Septal | 1 | NexPak X | |
| 4 | 00858439001330 | 9210584 | PosiSep X devices are patient-comfortable sponges manufactured from naturally oc PosiSep X devices are patient-comfortable sponges manufactured from naturally occurring Chitosan polymers. PosiSep X devices expand when hydrated providing separation between the sinus tissues. | EMX,LYA,FRO | Balloon, Epistaxis,Splint, Intranasal Septal,Dressing, Wound, Drug | PosiSep X 0.6 x 2.0 Hemostatic Dressing/Intranasal Splint | ||
| 5 | 00858439001309 | 9210574 | PosiSep devices are patient-comfortable sponges manufactured from naturally occu PosiSep devices are patient-comfortable sponges manufactured from naturally occurring Chitosan polymers. PosiSep devices expand when hydrated providing separation between the sinus tissues. | EMX,LYA,FRO | Balloon, Epistaxis,Splint, Intranasal Septal,Dressing, Wound, Drug | 1 | PosiSep 0.6 x 2.0 Hemostatic Dressing/Intranasal Splint | |
| 6 | 00858439001903 | 9210615 | PosiSep X2 devices are patient-comfortable sponges manufactured from naturally o PosiSep X2 devices are patient-comfortable sponges manufactured from naturally occurring Chitosan polymers. PosiSep X2 devices expand when hydrated providing separation between the sinus tissues. | LYA,EMX,FRO | Splint, Intranasal Septal,Balloon, Epistaxis,Dressing, Wound, Drug | 1 | PosiSep X2 0.8" x 2.3" | |
| 7 | 00858439001552 | 9550074 | The Hemostasis BoneSeal Bone Hemostat stops bone bleeding by establishing a phys The Hemostasis BoneSeal Bone Hemostat stops bone bleeding by establishing a physical barrier along the edges of bones that have been damaged by trauma or cut during a surgical procedure. When applied as directed, BoneSeal forms a mechanical barrier that occludes the vascular openings in the damaged bone. This barrier prevents further bleeding during the surgical procedure.BoneSeal is based upon known biodegradable polymeric chemistry that forms a ready-to-use hemostatic agent. BoneSeal is available as a bone hemostat ingot of various masses. The bone hemostat ingot can be molded and formed by the surgeon to fit the damaged bone and applied to the bleeding area. | MTJ | Wax, Bone | U | BoneSeal 2x2.5 gram Ingot | |
| 8 | 00858439001361 | 9210604 | PosiSep X devices are patient-comfortable sponges manufactured from naturally oc PosiSep X devices are patient-comfortable sponges manufactured from naturally occurring Chitosan polymers. PosiSep X devices expand when hydrated providing separation between the sinus tissues. | EMX,LYA,FRO | Balloon, Epistaxis,Splint, Intranasal Septal,Dressing, Wound, Drug | 1 | PosiSep X 8.0 cm x 1.8 cm Hemostatic Dressing/Intranasal Splint | |
| 9 | 00858439001972 | 9130154 | The Hemostasis NexStat topical hemostat powder is a sterile, topical wound dress The Hemostasis NexStat topical hemostat powder is a sterile, topical wound dressing comprised of plant based polysaccharides. The hemostatic particles quickly dehydrate blood cells, resulting in hemoconcentration of platelets, serum proteins and fibrinogen, leading to clotting that limits and controls bleeding. | FRO | Dressing, Wound, Drug | U | NexStat 1gm | |
| 10 | 00858439001538 | 9550054 | The Hemostasis BoneSeal Bone Hemostat stops bone bleeding by establishing a phys The Hemostasis BoneSeal Bone Hemostat stops bone bleeding by establishing a physical barrier along the edges of bones that have been damaged by trauma or cut during a surgical procedure. When applied as directed, BoneSeal forms a mechanical barrier that occludes the vascular openings in the damaged bone. This barrier prevents further bleeding during the surgical procedure.BoneSeal is based upon known biodegradable polymeric chemistry that forms a ready-to-use hemostatic agent. BoneSeal is available as a bone hemostat ingot of various masses. The bone hemostat ingot can be molded and formed by the surgeon to fit the damaged bone and applied to the bleeding area. | MTJ | Wax, Bone | U | BoneSeal 2.5 gram Ingot | |
| 11 | 00858439001880 | 9210614 | PosiSep X2 devices are patient-comfortable sponges manufactured from naturally o PosiSep X2 devices are patient-comfortable sponges manufactured from naturally occurring Chitosan polymers. PosiSep X2 devices expand when hydrated providing separation between the sinus tissues. | LYA,EMX,FRO | Splint, Intranasal Septal,Balloon, Epistaxis,Dressing, Wound, Drug | PosiSep X2 0.7" x 1.7" | ||
| 12 | 00858439001613 | 9110524 | NexPak Intranasal Splint is a sterile flexible foam pad comprised of a lyophiliz NexPak Intranasal Splint is a sterile flexible foam pad comprised of a lyophilized mixture of starch polysaccharide and polysaccharide binders. NexPak Intranasal Splint is intended to minimize bleeding and edema and to prevent adhesions between the septum and nasal cavity. The intranasal splint is placed in the nasal cavity after surgery or trauma. | LYA | Splint, Intranasal Septal | 1 | NexPak | |
| 13 | 00858439001514 | 9550034 | The Hemostasis BoneSeal Bone Hemostat stops bone bleeding by establishing a phys The Hemostasis BoneSeal Bone Hemostat stops bone bleeding by establishing a physical barrier along the edges of bones that have been damaged by trauma or cut during a surgical procedure. When applied as directed, BoneSeal forms a mechanical barrier that occludes the vascular openings in the damaged bone. This barrier prevents further bleeding during the surgical procedure.BoneSeal is based upon known biodegradable polymeric chemistry that forms a ready-to-use hemostatic agent. BoneSeal is available as a bone hemostat ingot of various masses. The bone hemostat ingot can be molded and formed by the surgeon to fit the damaged bone and applied to the bleeding area. | MTJ | Wax, Bone | BoneSeal 3.5 gram Ingot | ||
| 14 | 00858439001385 | 9210754 | PosiSep C devices are patient-comfortable sponges manufactured from naturally oc PosiSep C devices are patient-comfortable sponges manufactured from naturally occurring Chitosan polymers. PosiSep C devices were specifically engineered for use as a nasal dressing to be used following clinic based procedures. | EMX,LYA | Balloon, Epistaxis,Splint, Intranasal Septal | 1 | PosiSep C | |
| 15 | 00858439001323 | 9430034 | The hemostasis NexStat Plus topical hemostat powder is a sterile, topical wound The hemostasis NexStat Plus topical hemostat powder is a sterile, topical wound dressing comprised of plant based polysaccharides. The hemostatic particles quickly dehydrate blood cells, resulting in hemoconcentration of platelets, serum proteins and fibrinogen, leading to clotting that limits and controls bleeding. | FRO | Dressing, Wound, Drug | U | NexStat Plus 3gm | |
| 16 | 00858439001699 | 9210223 | ExcelArrest XT (EAXT) is a single use, sterile, dry chitosan-based foam hemostat ExcelArrest XT (EAXT) is a single use, sterile, dry chitosan-based foam hemostat. EAXT is offered as compressed foam pads in sterile barrier pouches. | FRO | Dressing, Wound, Drug | U | ExcelArrest XT 2x2 Hemostatic Patch | |
| 17 | 00858439001279 | 9210564 | PosiSep X devices are patient-comfortable sponges manufactured from naturally oc PosiSep X devices are patient-comfortable sponges manufactured from naturally occurring Chitosan polymers. PosiSep X devices expand when hydrated providing separation between the sinus tissues. | EMX,LYA,FRO | Balloon, Epistaxis,Splint, Intranasal Septal,Dressing, Wound, Drug | 1 | PosiSep X 0.5 x 1.5 Hemostatic Dressing/Intranasal Splint | |
| 18 | 00858439001262 | 9430014 | The Hemostasis NexStat Plus topical hemostat powder is a sterile, topical wound The Hemostasis NexStat Plus topical hemostat powder is a sterile, topical wound dressing comprised of plant based polysaccharides. The hemostatic particles quickly dehydrate blood cells, resulting in hemoconcentration of platelets, serum proteins and fibrinogen, leading to clotting that limits and controls bleeding. | FRO | Dressing, Wound, Drug | U | NexStat Plus 2gm | |
| 19 | 00858439001248 | 9210554 | PosiSep devices are patient-comfortable sponges manufactured from naturally occu PosiSep devices are patient-comfortable sponges manufactured from naturally occurring Chitosan polymers. PosiSep devices expand when hydrated providing separation between the sinus tissues. | EMX,FRO,LYA | Balloon, Epistaxis,Dressing, Wound, Drug,Splint, Intranasal Septal | PosiSep 0.5 x 1.5 Hemostatic Dressing/Intranasal Splint | ||
| 20 | 00858439001453 | 9110254 | The Hemostasis NexFoam topical hemostat sponge is a sterile, topical wound dress The Hemostasis NexFoam topical hemostat sponge is a sterile, topical wound dressing comprised of plant based polysaccharides. The hemostatic particles quickly dehydrate blood cells, resulting in hemoconcentration of platelets, serum proteins and fibrinogen, leading to clotting that limits and controls bleeding. | FRO | Dressing, Wound, Drug | U | NexFoam | |
| 21 | 00858439001439 | 9130144 | The Hemostasis NexStat topical hemostat powder is a sterile, topical wound dress The Hemostasis NexStat topical hemostat powder is a sterile, topical wound dressing comprised of plant based polysaccharides. The hemostatic particles quickly dehydrate blood cells, resulting in hemoconcentration of platelets, serum proteins and fibrinogen, leading to clotting that limits and controls bleeding. | FRO | Dressing, Wound, Drug | NexStat | ||
| 22 | 00858439001415 | 9210764 | PosiSep C² devices are patient-comfortable sponges manufactured from naturally o PosiSep C² devices are patient-comfortable sponges manufactured from naturally occurring Chitosan polymers. PosiSep C² devices were specifically engineered for use as a nasal dressing to be used following clinic based procedures. | EMX,LYA | Balloon, Epistaxis,Splint, Intranasal Septal | 1 | PosiSep C² |
| No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
|---|---|---|---|---|---|---|
| 1 | 10888277723863 | CSG50TUBE | CSG50TUBE | PLUROGEL WITH PHMB, 50G,1.75OZ TUBE | Medline | MEDLINE INDUSTRIES, INC. |
| 2 | 10888277692329 | NON266025 | NON266025 | GAUZE,PACKING STRIP,IODOFORM,2"X5YD,STRL | Medline | MEDLINE INDUSTRIES, INC. |
| 3 | 10885632127045 | SWF071 | Wound Flush Saline Spray 7.1 Ounce Sterile Not Made With Natural Rubber Latex MediChoice | MediChoice | OWENS & MINOR DISTRIBUTION, INC. | |
| 4 | 10885403430022 | 410123 | BD ChloraShield™ IV Nexiva™ Dressing with Chlorhexidine Gluconate (CHG) Antimicr BD ChloraShield™ IV Nexiva™ Dressing with Chlorhexidine Gluconate (CHG) Antimicrobial for BD Nexiva™ Closed Catheter Systems, 3.3 x 2.4 in (83 x 60 mm) | BD ChloraShield™ IV Nexiva™ Dressing with CHG Antimicrobial | AVERY DENNISON BELGIE BVBA | |
| 5 | 10885403288883 | 410132 | BD ChloraShield™ IV Surround Dressing with Chlorhexidine Gluconate (CHG) Antimic BD ChloraShield™ IV Surround Dressing with Chlorhexidine Gluconate (CHG) Antimicrobial, 4.0 x 4.3 in (10 x 11 cm) with notch. | BD ChloraShield™ IV Surround Dressing with CHG Antimicrobial | AVERY DENNISON BELGIE BVBA | |
| 6 | 10885403288876 | 410131 | BD ChloraShield™ IV Dressing with Chlorhexidine Gluconate (CHG) Antimicrobial, 4 BD ChloraShield™ IV Dressing with Chlorhexidine Gluconate (CHG) Antimicrobial, 4.0 x 4.3 in (10 x 11 cm) | BD ChloraShield™ IV Dressing with CHG Antimicrobial | AVERY DENNISON BELGIE BVBA | |
| 7 | 10885403284779 | 410122 | BD ChloraShield™ IV Surround Dressing with Chlorhexidine Gluconate (CHG) Antimic BD ChloraShield™ IV Surround Dressing with Chlorhexidine Gluconate (CHG) Antimicrobial, 3.0 x 2.4 in (75 x 60 mm) with slit. | BD ChloraShield™ IV Surround Dressing with CHG Antimicrobial | AVERY DENNISON BELGIE BVBA | |
| 8 | 10885403284762 | 410111 | BD ChloraShield™ IV Dressing with Chlorhexidine Gluconate (CHG) Antimicrobial, 3 BD ChloraShield™ IV Dressing with Chlorhexidine Gluconate (CHG) Antimicrobial, 3.0 x 2.4 in (75 x 60 mm) | BD ChloraShield™ IV Dressing with CHG Antimicrobial | AVERY DENNISON BELGIE BVBA | |
| 9 | 10885380115981 | ZSHG15 | ZSHG15 | Silver Amorphous Hydrogel; Silver; 1.575 oz Tube | CARDINAL HEALTH ESSENTIALS | RGH ENTERPRISES |
| 10 | 10885380065101 | RGFB812AG | RGFB812AG | Reinforced Gelling Fiber +Ag8 x 12 in. DressingPartial to full thickness wounds: Reinforced Gelling Fiber +Ag8 x 12 in. DressingPartial to full thickness wounds: -Pressure ulcers-Leg ulcers-Diabetic ulcers-Post-operative surgical wounds-First- and second-degree burns-Graft and donor sites-Trauma wounds (dermal lesions, trauma injuries or incisions)Highly absorbent gelling fibersCohesive fiber constructionEffective antimicrobial silverDirections for use: 1. Clean wound area with an appropriate wound cleanser such as Cardinal Health Wound Cleanser or normal saline solution. Dry surrounding skin thoroughly.2. Remove dressing from packaging and if necessary cut dressing to size using sterile scissors.3. Apply dressing over the wound bed leaving a 1/2-inch overlap. If wound is deep, loosely fill wound ensuring that the dressing does not overlap wound margins. Product will expand to fill the empty wound space once in contact with the exudate. Dressing can be pre-moistened with room temperature sterile water or saline solution before application.4. Cover wound and this primary dressing with a non-occlusive secondary dressing to promote a moist wound healing environment.5. All dressings should be monitored frequently. Remove dressing when clinically indicated, such as leakage, excessive bleeding, increased pain, or after a maximum of 7 days. IndicationsMay be used for the management of moderate to heavy exuding, partial to full thickness wounds including: -Pressure ulcers-Leg ulcers-Diabetic ulcers-Post-operative surgical wounds-First- and second-degree burns-Graft and donor sites-Trauma wounds (dermal lesions, trauma injuries or incisions) | CARDINAL HEALTH | CARDINAL HEALTH 200, LLC |
| 11 | 10885380065095 | RGFB66AG | RGFB66AG | Reinforced Gelling Fiber +Ag6 x 6 in. DressingPartial to full thickness wounds: Reinforced Gelling Fiber +Ag6 x 6 in. DressingPartial to full thickness wounds: -Pressure ulcers-Leg ulcers-Diabetic ulcers-Post-operative surgical wounds-First- and second-degree burns-Graft and donor sites-Trauma wounds (dermal lesions, trauma injuries or incisions)Highly absorbent gelling fibersCohesive fiber constructionEffective antimicrobial silverDirections for use: 1. Clean wound area with an appropriate wound cleanser such as Cardinal Health Wound Cleanser or normal saline solution. Dry surrounding skin thoroughly.2. Remove dressing from packaging and if necessary cut dressing to size using sterile scissors.3. Apply dressing over the wound bed leaving a 1/2-inch overlap. If wound is deep, loosely fill wound ensuring that the dressing does not overlap wound margins. Product will expand to fill the empty wound space once in contact with the exudate. Dressing can be pre-moistened with room temperature sterile water or saline solution before application.4. Cover wound and this primary dressing with a non-occlusive secondary dressing to promote a moist wound healing environment.5. All dressings should be monitored frequently. Remove dressing when clinically indicated, such as leakage, excessive bleeding, increased pain, or after a maximum of 7 days. IndicationsMay be used for the management of moderate to heavy exuding, partial to full thickness wounds including: -Pressure ulcers-Leg ulcers-Diabetic ulcers-Post-operative surgical wounds-First- and second-degree burns-Graft and donor sites-Trauma wounds (dermal lesions, trauma injuries or incisions) | CARDINAL HEALTH | CARDINAL HEALTH 200, LLC |
| 12 | 10885380065088 | RGFB45AG | RGFB45AG | Reinforced Gelling Fiber +Ag4 x 4.75 in. DressingPartial to full thickness wound Reinforced Gelling Fiber +Ag4 x 4.75 in. DressingPartial to full thickness wounds: -Pressure ulcers-Leg ulcers-Diabetic ulcers-Post-operative surgical wounds-First- and second-degree burns-Graft and donor sites-Trauma wounds (dermal lesions, trauma injuries or incisions)Highly absorbent gelling fibersCohesive fiber constructionEffective antimicrobial silverDirections for use: 1. Clean wound area with an appropriate wound cleanser such as Cardinal Health Wound Cleanser or normal saline solution. Dry surrounding skin thoroughly.2. Remove dressing from packaging and if necessary cut dressing to size using sterile scissors.3. Apply dressing over the wound bed leaving a 1/2-inch overlap. If wound is deep, loosely fill wound ensuring that the dressing does not overlap wound margins. Product will expand to fill the empty wound space once in contact with the exudate. Dressing can be pre-moistened with room temperature sterile water or saline solution before application.4. Cover wound and this primary dressing with a non-occlusive secondary dressing to promote a moist wound healing environment.5. All dressings should be monitored frequently. Remove dressing when clinically indicated, such as leakage, excessive bleeding, increased pain, or after a maximum of 7 days. IndicationsMay be used for the management of moderate to heavy exuding, partial to full thickness wounds including: -Pressure ulcers-Leg ulcers-Diabetic ulcers-Post-operative surgical wounds-First- and second-degree burns-Graft and donor sites-Trauma wounds (dermal lesions, trauma injuries or incisions) | CARDINAL HEALTH | CARDINAL HEALTH 200, LLC |
| 13 | 10885380065071 | RGFB22AG | RGFB22AG | Reinforced Gelling Fiber +Ag2 x 2 in. DressingPartial to full thickness wounds: Reinforced Gelling Fiber +Ag2 x 2 in. DressingPartial to full thickness wounds: -Pressure ulcers-Leg ulcers-Diabetic ulcers-Post-operative surgical wounds-First- and second-degree burns-Graft and donor sites-Trauma wounds (dermal lesions, trauma injuries or incisions)Highly absorbent gelling fibersCohesive fiber constructionEffective antimicrobial silverDirections for use: 1. Clean wound area with an appropriate wound cleanser such as Cardinal Health Wound Cleanser or normal saline solution. Dry surrounding skin thoroughly.2. Remove dressing from packaging and if necessary cut dressing to size using sterile scissors.3. Apply dressing over the wound bed leaving a 1/2-inch overlap. If wound is deep, loosely fill wound ensuring that the dressing does not overlap wound margins. Product will expand to fill the empty wound space once in contact with the exudate. Dressing can be pre-moistened with room temperature sterile water or saline solution before application.4. Cover wound and this primary dressing with a non-occlusive secondary dressing to promote a moist wound healing environment.5. All dressings should be monitored frequently. Remove dressing when clinically indicated, such as leakage, excessive bleeding, increased pain, or after a maximum of 7 days. IndicationsMay be used for the management of moderate to heavy exuding, partial to full thickness wounds including: -Pressure ulcers-Leg ulcers-Diabetic ulcers-Post-operative surgical wounds-First- and second-degree burns-Graft and donor sites-Trauma wounds (dermal lesions, trauma injuries or incisions) | CARDINAL HEALTH | CARDINAL HEALTH 200, LLC |
| 14 | 10885380065064 | RGFBROPEAG | RGFBROPEAG | Reinforced Gelling Fiber +Ag.75 x 18 in. RopePartial to full thickness wounds: - Reinforced Gelling Fiber +Ag.75 x 18 in. RopePartial to full thickness wounds: -Pressure ulcers-Leg ulcers-Diabetic ulcers-Post-operative surgical wounds-First- and second-degree burns-Graft and donor sites-Trauma wounds (dermal lesions, trauma injuries or incisions)Highly absorbent gelling fibersCohesive fiber constructionEffective antimicrobial silverDirections for use: 1. Clean wound area with an appropriate wound cleanser such as Cardinal Health Wound Cleanser or normal saline solution. Dry surrounding skin thoroughly.2. Remove dressing from packaging and if necessary cut dressing to size using sterile scissors.3. Apply dressing over the wound bed leaving a 1/2-inch overlap. If wound is deep, loosely fill wound ensuring that the dressing does not overlap wound margins. Product will expand to fill the empty wound space once in contact with the exudate. Dressing can be pre-moistened with room temperature sterile water or saline solution before application.4. Cover wound and this primary dressing with a non-occlusive secondary dressing to promote a moist wound healing environment.5. All dressings should be monitored frequently. Remove dressing when clinically indicated, such as leakage, excessive bleeding, increased pain, or after a maximum of 7 days. IndicationsMay be used for the management of moderate to heavy exuding, partial to full thickness wounds including: -Pressure ulcers-Leg ulcers-Diabetic ulcers-Post-operative surgical wounds-First- and second-degree burns-Graft and donor sites-Trauma wounds (dermal lesions, trauma injuries or incisions) | CARDINAL HEALTH | CARDINAL HEALTH 200, LLC |
| 15 | 10884527022489 | 55546BAMD | 55546BAMD | AMD Antimicrobial Foam Border Dressing,0.5% Polyhexamethylene Biguanide HCI (PHMB) | Kendall | CARDINAL HEALTH, INC. |
| 16 | 10884527022465 | 55566BAMD | 55566BAMD | AMD Antimicrobial Foam Border Dressing,0.5% Polyhexamethylene Biguanide HCI (PHMB) | Kendall | CARDINAL HEALTH, INC. |
| 17 | 10884527022458 | 55544BAMD | 55544BAMD | AMD Antimicrobial Foam Border Dressing,0.5% Polyhexamethylene Biguanide HCI (PHMB) | Kendall | CARDINAL HEALTH, INC. |
| 18 | 10884527014996 | 8884437305 | 8884437305 | Non-occlusive Roll,3% Bismuth Tribromophenate in Oil Emulsion | Xeroform | CARDINAL HEALTH, INC. |
| 19 | 10884527014989 | 8884437201 | 8884437201 | Non-occlusive Gauze Strip Overwrap,3% Bismuth Tribromophenate in Oil Emulsion | Xeroform | CARDINAL HEALTH, INC. |
| 20 | 10884527014972 | 8884437100 | 8884437100 | Non-occlusive Gauze Strip Overwrap,3% Bismuth Tribromophenate in Oil Emulsion | Xeroform | CARDINAL HEALTH, INC. |
| 21 | 10884527014965 | 8884436400 | 8884436400 | Non-occlusive Patch,3% Bismuth Tribromophenate in Oil Emulsion | Xeroform | CARDINAL HEALTH, INC. |
| 22 | 10884527014941 | 8884433500 | 8884433500 | Occlusive Gauze Patch,3% Bismuth Tribromophenate in Petrolatum Blend | Xeroform | CARDINAL HEALTH, INC. |
| 23 | 10884527014934 | 8884433400 | 8884433400 | Occlusive Gauze Patch,3% Bismuth Tribromophenate in Petrolatum Blend | Xeroform | CARDINAL HEALTH, INC. |
| 24 | 10884527014910 | 8884432000 | 8884432000 | Occlusive Gauze Roll,3% Bismuth Tribromophenate in Petrolatum Blend | Xeroform | CARDINAL HEALTH, INC. |
| 25 | 10884527014903 | 8884431605 | 8884431605 | Occlusive Gauze Strip Overwrap,3% Bismuth Tribromophenate in Petrolatum Blend | Xeroform | CARDINAL HEALTH, INC. |
| 26 | 10884527014897 | 8884431302 | 8884431302 | Occlusive Gauze Strip Overwrap,3% Bismuth Tribromophenate in Petrolatum Blend | Xeroform | CARDINAL HEALTH, INC. |
| 27 | 10884527014880 | 8884427601 | 8884427601 | Petrolatum Gauze Cision Dressing,Overwrap | Vaseline | CARDINAL HEALTH, INC. |
| 28 | 10884527014873 | 8884426600 | 8884426600 | Petrolatum Gauze Strip,Overwrap | Vaseline | CARDINAL HEALTH, INC. |
| 29 | 10884527014866 | 8884425600 | 8884425600 | Petrolatum Gauze Strip,Overwrap | Vaseline | CARDINAL HEALTH, INC. |
| 30 | 10884527014859 | 8884424600 | 8884424600 | Petrolatum Gauze Strip,Overwrap | Vaseline | CARDINAL HEALTH, INC. |
| 31 | 10884527014842 | 8884423600 | 8884423600 | Petrolatum Gauze Strip,Overwrap | Vaseline | CARDINAL HEALTH, INC. |
| 32 | 10884527014835 | 8884422600 | 8884422600 | Petrolatum Gauze Strip,Overwrap | Vaseline | CARDINAL HEALTH, INC. |
| 33 | 10884527014828 | 8884421600 | 8884421600 | Petrolatum Gauze Tube Foil,Overwrap | Vaseline | CARDINAL HEALTH, INC. |
| 34 | 10884527000340 | 10000 | 10000 | Sterile Water | Argyle | CARDINAL HEALTH, INC. |
| 35 | 10884527000319 | 1020 | 1020 | Sterile Saline, 0.9% | Argyle | CARDINAL HEALTH, INC. |
| 36 | 10884521551206 | 55599BAMDG | 55599BAMDG | AMD Antimicrobial Gentle Border Foam Sacrum 0.5% Polyhexamethylene Biguanide HCI (PHMB) | Kendall | CARDINAL HEALTH, INC. |
| 37 | 10884521551190 | 55577BAMDG | 55577BAMDG | AMD Antimicrobial Gentle Border Foam Sacrum 0.5%; Polyhexamethylene Biguanide HCI (PHMB) | Kendall | CARDINAL HEALTH, INC. |
| 38 | 10884521537446 | 1024 | 1024 | Sterile Water | Argyle | CARDINAL HEALTH, INC. |
| 39 | 10884521537439 | 1022 | 1022 | Sterile Saline, 0.9% | Argyle | CARDINAL HEALTH, INC. |
| 40 | 10884521177291 | 55588BAMDX | 55588BAMDX | AMD Antimicrobial Foam Border Dressing,0.5% Polyhexamethylene Biguanide HCI (PHMB) | Kendall | CARDINAL HEALTH, INC. |
| 41 | 10884521177284 | 55566BAMDX | 55566BAMDX | AMD Antimicrobial Foam Border Dressing,0.5% Polyhexamethylene Biguanide HCI (PHMB) | Kendall | CARDINAL HEALTH, INC. |
| 42 | 10884521177277 | 55546BAMDX | 55546BAMDX | AMD Antimicrobial Foam Border Dressing,0.5% Polyhexamethylene Biguanide HCI (PHMB) | Kendall | CARDINAL HEALTH, INC. |
| 43 | 10884521177260 | 55544BAMDX | 55544BAMDX | AMD Antimicrobial Foam Border Dressing,0.5% Polyhexamethylene Biguanide HCI (PHMB) | Kendall | CARDINAL HEALTH, INC. |
| 44 | 10884521177253 | 55523BAMDX | 55523BAMDX | AMD Antimicrobial Foam Border Dressing,0.5% Polyhexamethylene Biguanide HCI (PHMB) | Kendall | CARDINAL HEALTH, INC. |
| 45 | 10884521140943 | 90SAL | 90SAL | Sterile Saline Wound Solution | Kendall | CARDINAL HEALTH, INC. |
| 46 | 10884521135765 | 8884433205 | 8884433205 | True content to be populated as part of rebranding | Vaseline | CARDINAL HEALTH, INC. |
| 47 | 10884521066007 | 55544AMD | 55544AMD | AMD Antimicrobial Foam Dressing,0.5% Polyhexamethylene Biguanide HCI (PHMB) | Kendall | CARDINAL HEALTH, INC. |
| 48 | 10884521065918 | 55544PAMD | 55544PAMD | AMD Antimicrobial Foam Dressing with Top Sheet,0.5% Polyhexamethylene Biguanide HCI (PHMB) | Kendall | CARDINAL HEALTH, INC. |
| 49 | 10884521065796 | 55548AMD | 55548AMD | AMD Antimicrobial Foam Dressing,0.5% Polyhexamethylene Biguanide HCI (PHMB) | Kendall | CARDINAL HEALTH, INC. |
| 50 | 10884521065741 | 55535AMD | 55535AMD | AMD Antimicrobial Fenestrated Foam Dressing,0.5% Polyhexamethylene Biguanide HCI (PHMB) | Kendall | CARDINAL HEALTH, INC. |