Primary Device ID | 00350770005843 |
NIH Device Record Key | a26480c8-3415-40ce-9e9a-4773a93aaf11 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Cortrak 2 Enternal access device |
Version Model Number | 20-0950 |
Catalog Number | 20-0950 |
Company DUNS | 079375431 |
Company Name | Avanos Medical, Inc. |
Device Count | 1 |
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 | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 18444282667 |
PIQ@AVANOS.COM | |
Phone | 18444282667 |
PIQ@AVANOS.COM | |
Phone | 18444282667 |
PIQ@AVANOS.COM | |
Phone | 18444282667 |
PIQ@AVANOS.COM | |
Phone | 18444282667 |
PIQ@AVANOS.COM | |
Phone | 18444282667 |
PIQ@AVANOS.COM | |
Phone | 18444282667 |
PIQ@AVANOS.COM | |
Phone | 18444282667 |
PIQ@AVANOS.COM | |
Phone | 18444282667 |
PIQ@AVANOS.COM | |
Phone | 18444282667 |
PIQ@AVANOS.COM | |
Phone | 18444282667 |
PIQ@AVANOS.COM | |
Phone | 18444282667 |
PIQ@AVANOS.COM | |
Phone | 18444282667 |
PIQ@AVANOS.COM | |
Phone | 18444282667 |
PIQ@AVANOS.COM |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00350770005843 [Primary] |
KNT | Tubes, Gastrointestinal (And Accessories) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-09-27 |
Device Publish Date | 2024-09-19 |
00350770005867 | P20-0950 |
00350770005843 | 20-0950 |
00350770005836 | 20-0950 |