| Primary Device ID | 20884527016157 | 
| NIH Device Record Key | 1f0995d3-0053-4c8b-97d6-22305f8d9731 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | Devon | 
| Version Model Number | 31142113 | 
| Catalog Number | 31142113 | 
| Company DUNS | 080935429 | 
| Company Name | Cardinal Health, Inc. | 
| Device Count | 1 | 
| DM Exempt | false | 
| Pre-market Exempt | true | 
| 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 | 
| Special Storage Condition, Specify | Between 0 and 0 *; | 
| Special Storage Condition, Specify | Between 0 and 0 *; | 
| Special Storage Condition, Specify | Between 0 and 0 *; | 
| Special Storage Condition, Specify | Between 0 and 0 *; | 
| Special Storage Condition, Specify | Between 0 and 0 *; | 
| Special Storage Condition, Specify | Between 0 and 0 *; | 
| Special Storage Condition, Specify | Between 0 and 0 *; | 
| Special Storage Condition, Specify | Between 0 and 0 *; | 
| Special Storage Condition, Specify | Between 0 and 0 *; | 
| Special Storage Condition, Specify | Between 0 and 0 *; | 
| Special Storage Condition, Specify | Between 0 and 0 *; | 
| Special Storage Condition, Specify | Between 0 and 0 *; | 
| Special Storage Condition, Specify | Between 0 and 0 *; | 
| Special Storage Condition, Specify | Between 0 and 0 *; | 
| Special Storage Condition, Specify | Between 0 and 0 *; | 
| Special Storage Condition, Specify | Between 0 and 0 *; | 
| Special Storage Condition, Specify | Between 0 and 0 *; | 
| Special Storage Condition, Specify | Between 0 and 0 *; | 
| Special Storage Condition, Specify | Between 0 and 0 *; | 
| Special Storage Condition, Specify | Between 0 and 0 *; | 
| Special Storage Condition, Specify | Between 0 and 0 *; | 
| Special Storage Condition, Specify | Between 0 and 0 *; | 
| Special Storage Condition, Specify | Between 0 and 0 *; | 
| Special Storage Condition, Specify | Between 0 and 0 *; | 
| Special Storage Condition, Specify | Between 0 and 0 *; | 
| Special Storage Condition, Specify | Between 0 and 0 *; | 
| Special Storage Condition, Specify | Between 0 and 0 *; | 
| Special Storage Condition, Specify | Between 0 and 0 *; | 
| Special Storage Condition, Specify | Between 0 and 0 *; | 
| Special Storage Condition, Specify | Between 0 and 0 *; | 
| Special Storage Condition, Specify | Between 0 and 0 *; | 
| Special Storage Condition, Specify | Between 0 and 0 *; | 
| Special Storage Condition, Specify | Between 0 and 0 *; | 
| Device Issuing Agency | Device ID | 
|---|---|
| GS1 | 10884527016150 [Package] Contains: 30884527016154 Package: PACK_OR_INNER_PACK [12 Units] In Commercial Distribution | 
| GS1 | 20884527016157 [Package] Contains: 30884527016154 Package: CASE [96 Units] In Commercial Distribution | 
| GS1 | 30884527016154 [Primary] | 
| GAB | NEEDLE, SUTURING, DISPOSABLE | 
| Steralize Prior To Use | false | 
| Device Is Sterile | true | 
| Public Version Status | Update | 
| Device Record Status | Published | 
| Public Version Number | 2 | 
| Public Version Date | 2019-02-15 | 
| Device Publish Date | 2018-06-23 | 
| 10884527020171 | Suture Removal Kit,7044 Suture Removal Kit | 
| 20884527020154 | Suture Removal Kit,7042 Suture Removal Kit | 
| 10884527020140 | Suture Removal Kit,7046 Suture Removal Kit | 
| 20884527020062 | Suture Removal Kit,7044-MHH Suture Removal Kit | 
| 20884527016546 | 1822 Foam Block Needle Counter | 
| 20884527016539 | 1820 Foam Block Needle Counter | 
| 10884527016525 | 1812 Foam Block Needle Counter | 
| 20884527016508 | 1880 Foam Block Needle Counter | 
| 20884527016492 | 1630 Foam Strip Needle Counter | 
| 10884527016471 | 1810 Foam Block Needle Counter | 
| 10884527016464 | 1100 Single Magnet Needle Counter,Black | 
| 20884527016454 | 1842 Foam Block Needle Counter | 
| 20884527016447 | 1910 Foam Block Needle Counter | 
| 20884527016423 | 1920 Foam Block Needle Counter | 
| 10884527016419 | 1930 Foam Block Needle Counter | 
| 10884527016402 | 1922 Foam Block Needle Counter | 
| 20884527016393 | 1960 Foam Block Needle Counter | 
| 20884527016317 | 1840 Foam Block Needle Counter | 
| 20884527016287 | 1330 Double Foam Strip Needle Counter | 
| 10884527016273 | 1614 Foam Strip Needle Counter | 
| 20884527016249 | 1540 Double Magnet Needle Counter,White | 
| 10884527016235 | 1105 Foam Strip Needle Counter | 
| 20884527016225 | 1360 Foam Strip Needle Counter | 
| 10884527016211 | 1200 Double Magnet Needle Counter,Black | 
| 10884527016204 | 1315 Foam Strip Needle Counter | 
| 10884527016198 | 1314 Foam Strip Needle Counter | 
| 10884527016181 | 1260 Double Magnet Needle Counter,Black | 
| 20884527016171 | 1230 Double Magnet Needle Counter,Black | 
| 10884527016167 | 1110 Single Magnet Needle Counter,Black | 
| 20884527016157 | 1530 Double Magnet Needle Counter,Black | 
| 20884527016041 | Skin Marker,Fine Tip | 
| 10884527015962 | Printed Medication Labels | 
| 20884527015952 | Utility Marker with Preprinted Labels | 
| 10884527015917 | Utility Marker Labels | 
| 10884527015900 | Anti-fog Solution,1910 Needle Counter | 
| 10884527015894 | Scope Adjustment Bag | 
| 20884527015884 | Anti-Fog Solution with Foam Pad | 
| 20884527015839 | Tube Holder,Fixed Touch Fasten Strap | 
| 10884527015825 | Tube Holder,Removable Touch Fasten Strap | 
| 20884527015815 | Blade Shield Scalpel Holder | 
| 10884527015801 | Instrument Pouch,Double Pocket | 
| 20884527015792 | Micro Tip Wipe | 
| 20884527011763 | Light Handle | 
| 10884527011742 | Scope Adjustment Bag | 
| 10884527011735 | Light Glove | 
| 20884527011718 | Light Glove | 
| 20884527011701 | Light Glove | 
| 20884527011695 | Light Handle | 
| 10884527011681 | Light Handle | 
| 10884527011629 | 7075 Staple Remover | 
| Mark Image Registration | Serial | Company Trademark Application Date | 
|---|---|
|  DEVON  98631766  not registered Live/Pending | Cardinal Health 529, LLC 2024-07-03 | 
|  DEVON  98278891  not registered Live/Pending | Hines Interests Limited Partnership 2023-11-20 | 
|  DEVON  98188439  not registered Live/Pending | DEVON GUITARS 2023-09-20 | 
|  DEVON  97211388  not registered Live/Pending | DEVCOR CAPITAL INC. 2022-01-10 | 
|  DEVON  88424843  not registered Live/Pending | Cardinal Health 529, LLC 2019-05-10 | 
|  DEVON  85802470  4453636 Live/Registered | ASCENT HEALTHCARE, LLC 2012-12-13 | 
|  DEVON  85382582  not registered Dead/Abandoned | BLACK KNIGHT HOLDINGS, LLC 2011-07-27 | 
|  DEVON  81040117  1040117 Dead/Cancelled | Advanco Inc. 0000-00-00 | 
|  DEVON  79063566  3712283 Dead/Cancelled | CHERVON (CHINA) TRADING CO., LTD. 2008-08-07 | 
|  DEVON  78610143  3076726 Live/Registered | HOULIHAN'S RESTAURANTS, INC. 2005-04-15 | 
|  DEVON  77859791  not registered Dead/Abandoned | Devon Motorworks, LLC 2009-10-28 | 
|  DEVON  77759825  3736845 Live/Registered | Devon Energy Corporation 2009-06-15 |