FDA UDI In Commercial Distribution 🇺🇸 United States

Kerlix

DI: 10884527023318 · Model: 6120 · Cardinal Health, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
10

Basic Information

Brand Name
Kerlix
Primary DI
10884527023318
Version / Model
6120
Catalog Number
6120
Company Name
Cardinal Health, Inc.
Labeler DUNS
080935429
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2018-06-27
Public Version
3
Public Version Date
2021-08-24
Public Version Status
Update
Public Device Record Key
5a56d2ba-55fb-45f9-9412-1c51a13f9397

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
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
48134 Woven gauze pad

Identifiers

Type ID
Package 20884527023315
Primary 10884527023318
Unit of Use 30884527023312

Customer Contacts

Device Sizes

Type Value Unit Text
Length 4 Inch
Width 4 Inch

Storage Conditions

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