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 |