FDA UDI In Commercial Distribution 🇺🇸 United States

Kerlix

DI: 10884527023264 · Model: 4032 · Cardinal Health, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
100

Basic Information

Brand Name
Kerlix
Primary DI
10884527023264
Version / Model
4032
Catalog Number
4032
Company Name
Cardinal Health, Inc.
Labeler DUNS
080935429
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2018-06-27
Public Version
4
Public Version Date
2023-09-11
Public Version Status
Update
Public Device Record Key
9d848d3e-5d82-45e6-9618-26749895655a
Distribution End Date
2025-12-31

Device Description

Sponges,12 Ply

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
No
Sterilization Prior Use
No

Product Codes

Code Name
NAB Gauze / sponge,nonresorbable for external use

GMDN Terms

Code Name
48134 Woven gauze pad

Identifiers

Type ID
Package 20884527023261
Primary 10884527023264
Unit of Use 30884527023268

Device Sizes

Type Value Unit Text
Width 4 Inch
Length 4 Inch

Storage Conditions

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