FDA UDI In Commercial Distribution 🇺🇸 United States

Kerlix

DI: 20192253046981 · Model: 6662 · Cardinal Health 200, LLC
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
2

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Basic Information

Brand Name
Kerlix
Primary DI
20192253046981
Version / Model
6662
Catalog Number
6662
Company Name
Cardinal Health 200, LLC
Labeler DUNS
961027315
Distribution Status
In Commercial Distribution
Device Count in Pkg
2
Record Status
Published
Publish Date
2025-09-24
Public Version
1
Public Version Date
2025-10-02
Public Version Status
New
Public Device Record Key
5942e681-e22a-431c-911d-997c90302851

Device Description

Kerlix AMD Antimicrobial Super Sponges Medium • 0.2% Polyhexamethylene Biguanide HCl (PHMB) 6 in. x 6.75 in. (15.2 cm x 17.1 cm)

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
Yes
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
No
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
NAD Dressing, wound, occlusive

GMDN Terms

Code Name
48129 Gauze strip, antimicrobial

Identifiers

Type ID
Package 50192253046982
Package 30192253046988
Primary 20192253046981
Unit of Use 10192253046984

Device Sizes

Type Value Unit Text
Width 15.2 Centimeter
Length 17.1 Centimeter