Primary Device ID | 00761887003316 |
NIH Device Record Key | cfd36db5-bcc7-466c-bd6a-16ab134b8f9e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Avanos |
Version Model Number | 3124 |
Catalog Number | 3124 |
Company DUNS | 073386039 |
Company Name | PRYOR PRODUCTS |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00761887003316 [Primary] |
FOX | Stand, Infusion |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2023-10-18 |
Device Publish Date | 2021-05-01 |
00761887001817 | 3520E |
00761887003903 | Avanos Convers Kit/Cortak/Halyard |
00761887003316 | Clamp receiver unit cover |
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 |