FDA UDI In Commercial Distribution 🇺🇸 United States

Kerlix

DI: 50192253066478 · Model: 6735 · Cardinal Health 200, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
96

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Basic Information

Brand Name
Kerlix
Primary DI
50192253066478
Version / Model
6735
Catalog Number
6735
Company Name
Cardinal Health 200, LLC
Labeler DUNS
961027315
Distribution Status
In Commercial Distribution
Device Count in Pkg
96
Record Status
Published
Publish Date
2025-05-07
Public Version
1
Public Version Date
2025-05-15
Public Version Status
New
Public Device Record Key
571fdd16-60b8-4806-bafd-42fbc819fcb1

Device Description

Kerlix Bandage Roll

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
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
48127 Woven gauze roll/sheet

Identifiers

Type ID
Unit of Use 10192253066470
Primary 50192253066478

Device Sizes

Type Value Unit Text
Width 3.4 Inch
Length 3.6 Yard