Primary Device ID | 00849554015401 |
NIH Device Record Key | 4a807b1f-a812-4da1-8454-eab58a142390 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ActiV.A.C.™ |
Version Model Number | M8275058/10V014 |
Catalog Number | M8275058/10V014 |
Company DUNS | 102726734 |
Company Name | KCI USA, INC. |
Device Count | 10 |
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 | true |
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 | 00849554015401 [Unit of Use] |
GS1 | 00849554015418 [Primary] |
GS1 | 00849554015425 [Primary] |
OMP | negative pressure wound therapy Powered suction pump |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-08-08 |
Device Publish Date | 2024-07-31 |
00878237001486 | 300 ml Canister (with Gel) for Activac Therapy System Fluid Path Sterile |
00849554001992 | 300 ml Canister (with Gel) for Activac Therapy System Fluid Path Sterile |
00849554015401 | ACTIV.A.C. CANISTER WITH GEL 10/CASE, ATHLONE, IH1078249, None, 3M REBRANDING, NON STERILE |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ACTIV.A.C. 78874179 3346030 Live/Registered |
KCI Licensing, Inc. 2006-05-02 |