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 |