Primary Device ID | 00849554002081 |
NIH Device Record Key | 52663e64-2f1a-4165-981b-f090c0012239 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | INFOV.A.C.™ |
Version Model Number | M8275071/5 M8275071/10 |
Company DUNS | 102726734 |
Company Name | KCI USA, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
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 | 00849554002036 [Package] Package: 5 Pack [5 Units] In Commercial Distribution |
GS1 | 00849554002043 [Package] Package: 10 Pack [10 Units] In Commercial Distribution |
GS1 | 00849554002081 [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 | 2018-08-20 |
Device Publish Date | 2016-09-05 |
00878237000915 | 500 ml Canister (without Gel) for Infovac and VAC Ulta Therapy Systems |
00878237000892 | 500 ml Canister (with Gel) for Infovac and VAC Ulta Therapy Systems |
00849554002081 | 500 ml Canister (without Gel) for Infovac and VAC Ulta Therapy Systems |
00849554002074 | 500 ml Canister (with Gel) for Infovac and VAC Ulta Therapy Systems |
00849554002067 | 1000 ml Canister (with Gel) for Infovac and VAC Ulta Therapy Systems |
00849554006799 | Infovac Therapy System |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
INFOV.A.C. 78863340 3345980 Live/Registered |
KCI Licensing, Inc. 2006-04-18 |