Primary Device ID | 00849554005358 |
NIH Device Record Key | aff040d6-6b5a-4e29-8f24-2a363cf4131d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PREVENA PLUS™ |
Version Model Number | PRE4001US |
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 | 00849554005358 [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 | 2018-09-10 |
Device Publish Date | 2016-09-24 |
00849554006768 | Prevena Plus 125 Therapy Unit Prevena Plus 125 Therapy Unit with Prevena Plus 150ml Canister |
00849554005358 | Prevena Plus Incision Management System |
00849554005310 | Prevena Plus 150 ml Canister |
00849554007819 | PREVENA PLUS™ 125 THERAPY UNIT (14-DAY) WITH PREVENA PLUS™ 150ML CANISTER |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() PREVENA PLUS 86758994 5087992 Live/Registered |
KCI LICENSING, INC. 2015-09-16 |