| Primary Device ID | 00849554015401 |
| NIH Device Record Key | 4a807b1f-a812-4da1-8454-eab58a142390 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ActiV.A.C.™ |
| Version Model Number | M8275058/10V014 |
| Catalog Number | M8275058/10V014 |
| Company DUNS | 102726734 |
| Company Name | KCI USA, INC. |
| Device Count | 10 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Unsafe |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00849554015401 [Unit of Use] |
| GS1 | 00849554015418 [Primary] |
| GS1 | 00849554015425 [Primary] |
| OMP | negative pressure wound therapy Powered suction pump |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-08-08 |
| Device Publish Date | 2024-07-31 |
| 00878237001486 | 300 ml Canister (with Gel) for Activac Therapy System Fluid Path Sterile |
| 00849554001992 | 300 ml Canister (with Gel) for Activac Therapy System Fluid Path Sterile |
| 00849554015401 | ACTIV.A.C. CANISTER WITH GEL 10/CASE, ATHLONE, IH1078249, None, 3M REBRANDING, NON STERILE |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() ACTIV.A.C. 78874179 3346030 Live/Registered |
KCI Licensing, Inc. 2006-05-02 |