| Primary Device ID | 50849554014034 |
| NIH Device Record Key | 1f6a601f-9bf9-459d-a634-be3020f930f3 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | 3M™ Veraflo™ |
| Version Model Number | ULTVFL05SM |
| Catalog Number | ULTVFL05SM |
| Company DUNS | 102726734 |
| Company Name | KCI USA, 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 | true |
| 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 | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10849554014036 [Primary] |
| GS1 | 50849554014034 [Package] Contains: 10849554014036 Package: BOX [5 Units] In Commercial Distribution |
| OMP | negative pressure wound therapy Powered suction pump |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-07-20 |
| Device Publish Date | 2023-07-12 |
| 50849554014072 | 3M™ V.A.C. Veraflo Cleanse Choice™ Dressing, ULTVCC05LG, Large, Cavilon Warning Label, 5/CS |
| 50849554014065 | 3M™ V.A.C. Veraflo Cleanse Choice™ Dressing, ULTVCC05MD, Medium, Cavilon Warning Label, 5/CS |
| 50849554014058 | 3M™ V.A.C. Veraflo™ Dressing, ULTVFL05LG, Large, Cavilon Warning Label, 5/CS |
| 50849554014041 | 3M™ V.A.C. Veraflo™ Dressing, ULTVFL05MD, Medium, Cavilon Warning Label, 5/CS |
| 50849554014034 | 3M™ V.A.C. Veraflo™ Dressing, ULTVFL05SM, Small, Cavilon Warning Label, 5/CS |
| 50849554014027 | 3M™ V.A.C. Veraflo Cleanse™ Dressing, ULTVCL05MD, Medium, Cavilon Warning Label, 5/CS |