Primary Device ID | 00849554003767 |
NIH Device Record Key | 90b80aab-6e4f-4c64-ab6a-b4c401b1e640 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | V.A.C.VIA™ GRANUFOAM™ |
Version Model Number | VIAGFM05 |
Company DUNS | 102726734 |
Company Name | KCI USA, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Conditional |
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 | 00849554002296 [Package] Package: 5 Pack [5 Units] In Commercial Distribution |
GS1 | 00849554003767 [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 | 4 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-09-05 |
00849554003774 | Vac Via Dressing Small |
00849554003767 | VAC VIA Dressing Medium Featuring a Granufoam Spiral Dressing |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() V.A.C.VIA 77846707 3887702 Live/Registered |
KCI Licensing, Inc. 2009-10-12 |