| Primary Device ID | 00849554008243 |
| NIH Device Record Key | d3687b39-c6dd-4012-884e-b6315b165330 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | 3M™ Vac® |
| Version Model Number | ULTDEV01/US |
| Catalog Number | ULTDEV01/US |
| Company DUNS | 102726734 |
| Company Name | KCI USA, INC. |
| Device Count | 1 |
| 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 | false |
| Lot Batch | false |
| Serial Number | true |
| Manufacturing Date | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | +1(800)228-3957 |
| 3Mhealthcarecompliance@mmm.com | |
| Phone | +1(800)228-3957 |
| 3Mhealthcarecompliance@mmm.com | |
| Phone | +1(800)228-3957 |
| 3Mhealthcarecompliance@mmm.com | |
| Phone | +1(800)228-3957 |
| 3Mhealthcarecompliance@mmm.com | |
| Phone | +1(800)228-3957 |
| 3Mhealthcarecompliance@mmm.com | |
| Phone | +1(800)228-3957 |
| 3Mhealthcarecompliance@mmm.com | |
| Phone | +1(800)228-3957 |
| 3Mhealthcarecompliance@mmm.com | |
| Phone | +1(800)228-3957 |
| 3Mhealthcarecompliance@mmm.com | |
| Phone | +1(800)228-3957 |
| 3Mhealthcarecompliance@mmm.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00849554008243 [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 | 2022-08-01 |
| Device Publish Date | 2022-07-22 |
| 00849554008366 | 3M™ Vac® Ulta Therapy Unit CAPULTDEV01/US |
| 00849554008243 | 3M™ Vac® Ulta Therapy Unit ULTDEV01/US |