Primary Device ID | 00849554001268 |
NIH Device Record Key | 915c7823-3832-49c4-8621-5d7fd263d036 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ABTHERA™ |
Version Model Number | 370605 |
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 | 00849554000223 [Package] Package: 5 PACK [5 Units] In Commercial Distribution |
GS1 | 00849554001268 [Primary] |
FTL | Mesh, Surgical, Polymeric |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2018-08-15 |
Device Publish Date | 2016-09-05 |
00849554001275 | Abthera Tubing Set |
00849554001268 | Abthera Open Abdomen Dressing |
00849554001237 | Abthera Active Abdominal Therapy |
00849554000247 | ABTHERA CANISTER |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() ABTHERA 86724164 4881716 Live/Registered |
KCI LICENSING, INC. 2015-08-13 |
![]() ABTHERA 77658058 3753222 Live/Registered |
KCI Licensing, Inc. 2009-01-28 |