| Primary Device ID | 00851587006080 |
| NIH Device Record Key | 3c9bdeae-9965-43e3-9af0-f5915b19987a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | AirWrap |
| Version Model Number | FIN-0005-01 |
| Catalog Number | FIN-0005-01 |
| Company DUNS | 961523441 |
| Company Name | Revmedx, 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 | 503-218-2172 |
| info@revmedx.com | |
| Phone | 503-218-2172 |
| info@revmedx.com | |
| Phone | 503-218-2172 |
| info@revmedx.com | |
| Phone | 503-218-2172 |
| info@revmedx.com | |
| Phone | 503-218-2172 |
| info@revmedx.com | |
| Phone | 503-218-2172 |
| info@revmedx.com | |
| Phone | 503-218-2172 |
| info@revmedx.com | |
| Phone | 503-218-2172 |
| info@revmedx.com | |
| Phone | 503-218-2172 |
| info@revmedx.com | |
| Phone | 503-218-2172 |
| info@revmedx.com |
| Width | 4 Inch |
| Width | 4 Inch |
| Width | 4 Inch |
| Width | 4 Inch |
| Width | 4 Inch |
| Width | 4 Inch |
| Width | 4 Inch |
| Width | 4 Inch |
| Width | 4 Inch |
| Width | 4 Inch |
| Special Storage Condition, Specify | Between 0 and 0 *Store at Room Temperature |
| Special Storage Condition, Specify | Between 0 and 0 *Store at Room Temperature |
| Special Storage Condition, Specify | Between 0 and 0 *Store at Room Temperature |
| Special Storage Condition, Specify | Between 0 and 0 *Store at Room Temperature |
| Special Storage Condition, Specify | Between 0 and 0 *Store at Room Temperature |
| Special Storage Condition, Specify | Between 0 and 0 *Store at Room Temperature |
| Special Storage Condition, Specify | Between 0 and 0 *Store at Room Temperature |
| Special Storage Condition, Specify | Between 0 and 0 *Store at Room Temperature |
| Special Storage Condition, Specify | Between 0 and 0 *Store at Room Temperature |
| Special Storage Condition, Specify | Between 0 and 0 *Store at Room Temperature |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00851587006080 [Primary] |
| MHW | Dressing, Compression |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2026-02-27 |
| Device Publish Date | 2023-01-17 |
| 00851587006080 - AirWrap | 2026-02-27Pressure bandage |
| 00851587006080 - AirWrap | 2026-02-27 Pressure bandage |
| 00851587006226 - XSTAT P30 | 2026-02-27 Hemostatic device for severe bleeding. Each device comprises 3 pouches containing minisponges. Each pouch contains a radiopaqu |
| 00851587006066 - XSTAT | 2019-04-05 A hemostatic device for severe bleeding. Each device comprises approximately 108 small hemostatic sponges individually marked wi |
| 00851587006042 - XSTAT | 2018-07-06 A hemostatic device for severe bleeding. Each device comprises approximately 38 small hemostatic sponges individually marked wit |
| 10851587006056 - XSTAT | 2018-07-06 A hemostatic device for severe bleeding. Each device comprises approximately 92 small hemostatic sponges individually marked wit |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() AIRWRAP 98437848 not registered Live/Pending |
Truxx Outfitters, LLC 2024-03-07 |
![]() AIRWRAP 87704613 not registered Live/Pending |
Dyson Technology Limited 2017-12-01 |
![]() AIRWRAP 85953016 4594038 Live/Registered |
REVMEDX, INC. 2013-06-06 |
![]() AIRWRAP 85439274 4240573 Live/Registered |
The Little Linen Company 2011-10-04 |
![]() AIRWRAP 76618912 not registered Dead/Abandoned |
Stretch Associates, Inc. 2004-11-02 |