FDA UDI In Commercial Distribution 🇺🇸 United States

Kerlix

DI: 10192253047059 · Model: 6730 · Cardinal Health 200, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
Kerlix
Primary DI
10192253047059
Version / Model
6730
Catalog Number
6730
Company Name
Cardinal Health 200, LLC
Labeler DUNS
961027315
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-10-23
Public Version
1
Public Version Date
2024-10-31
Public Version Status
New
Public Device Record Key
f513a4f2-b58a-44c8-afde-f754b37c360f

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
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
Yes
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
Package 50192253047057
Primary 10192253047059

Device Sizes

Type Value Unit Text
Width 4.5 Inch
Length 4.1 Yard