FDA UDI In Commercial Distribution 🇺🇸 United States

Kerlix

DI: 20192253048244 · Model: 1167 · Cardinal Health 200, LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
100

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Basic Information

Brand Name
Kerlix
Primary DI
20192253048244
Version / Model
1167
Catalog Number
1167
Company Name
Cardinal Health 200, LLC
Labeler DUNS
961027315
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2025-03-19
Public Version
2
Public Version Date
2025-04-18
Public Version Status
Update
Public Device Record Key
b7952310-852d-4893-a448-966d939b7273

Device Description

Kerlix Super Sponges, Medium

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
No
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
No
Has Donation ID
No

Sterilization

Is Sterile
No
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 50192253048245
Primary 20192253048244
Unit of Use 10192253048247