| Primary Device ID | 00849554008090 |
| NIH Device Record Key | c19c087f-6e5a-425f-8511-7e1cf15add34 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | DERMATAC™ DRAPE and V.A.C.® GRANUFOAM™ DRESSING |
| Version Model Number | DTGF10PKL |
| Catalog Number | DTGF10PKL |
| Company DUNS | 102726734 |
| Company Name | KCI USA, INC. |
| Device Count | 10 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Safe |
| 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 | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00849554008090 [Unit of Use] |
| GS1 | 00849554009035 [Primary] |
| GS1 | 00849554009066 [Primary] |
| OMP | negative pressure wound therapy Powered suction pump |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2022-01-19 |
| Device Publish Date | 2022-01-06 |
| 00849554008090 | DERMATAC™ DRAPE and V.A.C.® GRANUFOAM™ LARGE DRESSING |
| 00849554008083 | DERMATAC™ DRAPE and V.A.C.® GRANUFOAM™ MEDIUM DRESSING |
| 00849554008076 | DERMATAC™ DRAPE and V.A.C.® GRANUFOAM™ SMALL DRESSING |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() DERMATAC 88111226 5909805 Live/Registered |
KCI LICENSING, INC. 2018-09-10 |
![]() DERMATAC 86283195 not registered Dead/Abandoned |
KCI LICENSING, INC. 2014-05-16 |
![]() DERMATAC 78266489 not registered Dead/Abandoned |
Surgical Specialties Corporation 2003-06-24 |