Primary Device ID | 00849554002388 |
NIH Device Record Key | 2b67e451-2a58-48af-b616-1a196cbcfec4 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | V.A.C.VIA™ |
Version Model Number | VIAKIT077D01/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 | 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 | 00849554002388 [Primary] |
OMP | Negative Pressure Wound Therapy Powered Suction Pump |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-08-20 |
Device Publish Date | 2016-09-05 |
00849554003750 | VAC VIA 250ml Canister |
00849554003156 | VAC Via System Starter Kit |
00849554002388 | VAC Via System 7-Day Kit |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() V.A.C.VIA 77846707 3887702 Live/Registered |
KCI Licensing, Inc. 2009-10-12 |