| Primary Device ID | 08056093720723 |
| NIH Device Record Key | bb327f4c-5f8d-4390-9ed3-6a8c4d56b453 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | AVANOS |
| Version Model Number | 44252 |
| Catalog Number | 7149-00 |
| Company DUNS | 429471691 |
| Company Name | CEDIC SRL |
| Device Count | 200 |
| 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 | false |
| OTC Over-The-Counter | false |
| Phone | +1(844)428-2667 |
| PIQ@AVANOS.COM |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 08056093720723 [Primary] |
| GS1 | 90680651442522 [Unit of Use] |
| PIO | Enteral specific transition connectors |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2019-11-22 |
| Device Publish Date | 2019-08-20 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() AVANOS 90629683 not registered Live/Pending |
AVANOS LLC 2021-04-07 |
![]() AVANOS 88027718 not registered Live/Pending |
Avent, Inc. 2018-07-06 |
![]() AVANOS 88027704 not registered Live/Pending |
Avent, Inc. 2018-07-06 |
![]() AVANOS 87911144 not registered Live/Pending |
Avent, Inc. 2018-05-08 |
![]() AVANOS 75484693 not registered Dead/Abandoned |
Biz411 Technologies, Inc. 1998-05-13 |