FDA UDI Not in Commercial Distribution 🇺🇸 United States

Kerlix

DI: 10884521058507 · Model: 6735 · Cardinal Health, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
96

Basic Information

Brand Name
Kerlix
Primary DI
10884521058507
Version / Model
6735
Catalog Number
6735
Company Name
Cardinal Health, Inc.
Labeler DUNS
080935429
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
96
Record Status
Published
Publish Date
2018-06-30
Public Version
5
Public Version Date
2023-07-03
Public Version Status
Update
Public Device Record Key
029ca673-c176-484b-aee5-b9b69d6a95e0
Distribution End Date
2023-07-01

Device Description

Bandage Roll,100% Cotton, 6 Ply, Medium

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
No
Sterilization Prior Use
No

Product Codes

Code Name
NAB Gauze / sponge,nonresorbable for external use

GMDN Terms

Code Name
48126 Woven gauze roll, non-sterile

Identifiers

Type ID
Primary 10884521058507
Unit of Use 20884521058504

Customer Contacts

Device Sizes

Type Value Unit Text
Width 3.4375 Inch
Length 3.1875 Feet

Storage Conditions

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