FDA UDI In Commercial Distribution 🇺🇸 United States

Kerlix

DI: 10884521058514 · Model: 6760 · Cardinal Health, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
5

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Basic Information

Brand Name
Kerlix
Primary DI
10884521058514
Version / Model
6760
Catalog Number
6760
Company Name
Cardinal Health, Inc.
Labeler DUNS
080935429
Distribution Status
In Commercial Distribution
Device Count in Pkg
5
Record Status
Published
Publish Date
2018-06-29
Public Version
4
Public Version Date
2025-04-18
Public Version Status
Update
Public Device Record Key
c0d7eb85-02b9-4d33-a436-c25b4612d488

Device Description

Bandage Roll Burn Pack,100% Cotton

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
48134 Woven gauze pad, non-antimicrobial

Identifiers

Type ID
Package 20884521058511
Primary 10884521058514
Unit of Use 30884521058518

Customer Contacts

Device Sizes

Type Value Unit Text
Width 4.50 Inch
Device Size Text, specify Length,4.125,yard;

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
This side up;