| Primary Device ID | 30884521024810 |
| NIH Device Record Key | 47f7d5f3-f8ec-4d68-8697-0105c4168d7f |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Kendall |
| Version Model Number | 9231 |
| Catalog Number | 9231 |
| Company DUNS | 080935429 |
| Company Name | Cardinal Health, Inc. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | true |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com |
| Length | 12 Inch |
| Length | 12 Inch |
| Length | 12 Inch |
| Length | 12 Inch |
| Length | 12 Inch |
| Length | 12 Inch |
| Length | 12 Inch |
| Length | 12 Inch |
| Length | 12 Inch |
| Length | 12 Inch |
| Length | 12 Inch |
| Length | 12 Inch |
| Length | 12 Inch |
| Length | 12 Inch |
| Length | 12 Inch |
| Length | 12 Inch |
| Length | 12 Inch |
| Length | 12 Inch |
| Length | 12 Inch |
| Length | 12 Inch |
| Length | 12 Inch |
| Length | 12 Inch |
| Length | 12 Inch |
| Length | 12 Inch |
| Length | 12 Inch |
| Length | 12 Inch |
| Length | 12 Inch |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10884521024816 [Package] Package: CASE [20 Units] In Commercial Distribution |
| GS1 | 20884521024813 [Package] Package: PACK_OR_INNER_PACK [5 Units] In Commercial Distribution |
| GS1 | 30884521024810 [Primary] |
| KMF | BANDAGE, LIQUID |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 7 |
| Public Version Date | 2019-03-25 |
| Device Publish Date | 2015-04-27 |
| 00884521152765 | Antimicrobial Bandage Roll |
| 00884521152185 | Antimicrobial Gauze Sponges |
| 20884521168678 | Fluff Underpad,X-Large,Moderate |
| 00884521167066 | Foam Border Gentle Adhesion,6 Inch x 6 Inch (15.2 cm x 15.2 cm) Pad |
| 00884521167004 | Foam Border Gentle Adhesion,4 Inch x 4 Inch (10.2 cm x 10.2 cm) Pad |
| 00884521166953 | Foam Border Gentle Adhesion,2 Inch x 4 Inch (5.1 cm x 10.2 cm) Pad |
| 00884521166908 | Foam Border Gentle Adhesion,2 Inch x 2 Inch (5.1 cm x 5.1 cm) Pad |
| 00884521166830 | Foam Border Gentle Adhesion,1 Inch x 1-3/4 Inch (2.5 cm x 4.4 cm) Pad |
| 00884521157159 | Stretch Bandage |
| 00884521157128 | Stretch Bandage |
| 00884521157104 | Stretch Bandage |
| 00884521152154 | Bandage Roll |
| 00884521170783 | Bandage Roll |
| 00884521153069 | Antimicrobial Non-adherent Pad |
| 00884521170790 | Antimicrobial Non-adherent Pad |
| 00884521152833 | Antimicrobial Adhesive Bandage |
| 00884521152741 | Antimicrobial Non-adherent Island Dressing |
| 00884521195939 | Alcohol Prep |
| 00884521065904 | AMD Antimicrobial Fenestrated Foam Dressing with Top Sheet,0.5% Polyhexamethylene Biguanide HCI |
| 00884521020880 | Hydrophilic Foam Plus Dressing,Fenestrated |
| 90884521148136 | 3000 Isolation Chamber,Rectal |
| 90884521148112 | 3100C Apnea Products |
| 10884527004737 | 7305 Foam Electrodes,Conductive Adhesive Hydrogel |
| 20884521057941 | Hydrogel Wound Dressing,Disc |
| 20884521024097 | Alginate Hydrocolloid Dressing,Border |
| 30884521021918 | Hydrogel Impregnated Gauze,USP Type VII Gauze Pad 0.25 oz (7 mL) Gel |
| 50884521020960 | Hydrophilic Foam Island Dressing,4 inch x 4 inch (10.2 cm x 10.2 cm) Pad |
| 20884521007540 | Transparent Film Dressing,Moisture Vapor Permeable |
| 20884527021793 | DL Disposable Cable and Lead Wire System,5 Lead Dual Connect, Adapter Required |
| 20884527021786 | DL Disposable Cable and Lead Wire System |
| 20884527021779 | DL Disposable Cable and Lead Wire System |
| 10884527021765 | DL Disposable Cable and Lead System |
| 10884527021758 | DL Disposable Lead System |
| 10884527021741 | DL Disposable Lead System |
| 20884527021731 | DL Disposable Lead System |
| 10884527021727 | DL Disposable Direct Connect |
| 20884527021717 | DL Disposable Direct Connect |
| 20884527021700 | DL Disposable Chest Leads |
| 10884527021697 | DL Disposable Cable and Lead Wire System,10 Lead, Adapter Required |
| 20884527021687 | DL Disposable Cable and Lead Wire System,5 Lead, Adapter Required |
| 10884527021673 | DL Disposable Cable and Lead Wire System,3 Lead, Adapter Required |
| 20884527017284 | Ultrasound Gel Bottle |
| 30884527015607 | 20661 Adult Multi-Function Defibrillation Electrodes,Radiotransparent |
| 10884527007875 | Wet Gel Electrodes,GC-11 Foam |
| 10884527007851 | 4603 Cloth Wet Gel Electrodes |
| 20884527005878 | 530 Foam Electrodes,Conductive Adhesive Hydrogel |
| 20884527004901 | Intrauterine Pressure Catheter,Transducer Tipped, Dual Lumen |
| 10884527004874 | SF450 Foam Electrodes,Conductive Adhesive Hydrogel |
| 10884527004843 | AC303 Cloth Electrodes,Repositionable, Conductive Adhesive Hydrogel |
| 20884527004833 | H69P Cloth Electrodes,Repositionable, Conductive Adhesive Hydrogel |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() KENDALL 98807100 not registered Live/Pending |
Homes For Life Decor Ltd. 2024-10-17 |
![]() KENDALL 90591223 not registered Live/Pending |
SHENZHEN FZONE TECHNOLOGY CO LIMITED 2021-03-19 |
![]() KENDALL 88660378 not registered Live/Pending |
Bemis Manufacturing Company 2019-10-18 |
![]() KENDALL 88413516 not registered Live/Pending |
Kendall Jenner, Inc. 2019-05-02 |
![]() KENDALL 87082661 5292342 Live/Registered |
Phillips 66 Company 2016-06-24 |
![]() KENDALL 86764949 not registered Dead/Abandoned |
AMERICAN GIRL, LLC 2015-09-22 |
![]() KENDALL 86584671 5138125 Live/Registered |
Kendall Jenner, Inc. 2015-04-01 |
![]() KENDALL 86584660 4999443 Live/Registered |
Kendall Jenner, Inc. 2015-04-01 |
![]() KENDALL 86069210 4587484 Live/Registered |
Covidien LP 2013-09-19 |
![]() KENDALL 85782377 5027358 Live/Registered |
KPR U.S., LLC 2012-11-19 |
![]() KENDALL 85401641 not registered Dead/Abandoned |
Abercrombie & Fitch Trading Co. 2011-08-18 |
![]() KENDALL 85335914 4117666 Live/Registered |
Kendall Electric, Inc. 2011-06-02 |