FDA UDI In Commercial Distribution 🇺🇸 United States

Kerlix

DI: 10192253047004 · Model: 6715 · Cardinal Health 200, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Kerlix
Primary DI
10192253047004
Version / Model
6715
Catalog Number
6715-
Company Name
Cardinal Health 200, LLC
Labeler DUNS
961027315
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-08-13
Public Version
1
Public Version Date
2024-08-21
Public Version Status
New
Public Device Record Key
5526cfd8-d7ef-4784-b62f-def53d9e5413

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
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
48127 Woven gauze roll/sheet

Identifiers

Type ID
Package 50192253047002
Primary 10192253047004

Device Sizes

Type Value Unit Text
Length 4.1 Yard
Width 4.5 Inch