FDA UDI In Commercial Distribution 🇺🇸 United States

Kerlix

DI: 20192253047582 · Model: 7884 · Cardinal Health 200, LLC
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
2

Basic Information

Brand Name
Kerlix
Primary DI
20192253047582
Version / Model
7884
Catalog Number
7884
Company Name
Cardinal Health 200, LLC
Labeler DUNS
961027315
Distribution Status
In Commercial Distribution
Device Count in Pkg
2
Record Status
Published
Publish Date
2025-09-23
Public Version
1
Public Version Date
2025-10-01
Public Version Status
New
Public Device Record Key
32268bbb-dfeb-456d-a2d8-bfde70488e65

Device Description

Kerlix Super Sponges

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
NAB Gauze / sponge,nonresorbable for external use

GMDN Terms

Code Name
48134 Woven gauze pad, non-antimicrobial

Identifiers

Type ID
Package 50192253047583
Package 30192253047589
Primary 20192253047582
Unit of Use 10192253047585

Device Sizes

Type Value Unit Text
Width 15 Centimeter
Length 17 Centimeter