Primary Device ID | 20192253047063 |
NIH Device Record Key | a6f0c278-a247-4dbe-bd0c-1c07b5daa060 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Webcol |
Version Model Number | 6818 |
Catalog Number | 6818- |
Company DUNS | 961027315 |
Company Name | Cardinal Health 200, LLC |
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 | true |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | false |
OTC Over-The-Counter | true |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10192253047066 [Primary] |
GS1 | 20192253047063 [Package] Contains: 10192253047066 Package: Carton [200 Units] In Commercial Distribution |
GS1 | 50192253047064 [Package] Package: CASE [20 Units] In Commercial Distribution |
LKB | Pad, alcohol, device disinfectant |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-06-18 |
Device Publish Date | 2025-06-10 |
10192253047097 | Alcohol Prep, 2 Ply, Medium |
20192253047063 | Alcohol Prep, 2 Ply, Medium, Made in USA, Saturated with 70% Isopropyl Alcohol, For external use |
10192253045727 | Alcohol Prep, 2 Ply, Medium |
50192253047071 | Skin Cleansing Alcohol Prep 2 ply Medium Saturated with 70% Isopropyl Alcohol |
50192253045749 | Alcohol Prep, 2 Ply, Large |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() WEBCOL 74011935 1624306 Dead/Cancelled |
VERATEC, INC. 1989-12-18 |
![]() WEBCOL 72147832 0747513 Live/Registered |
Kendall Company, The 1962-06-27 |