FDA UDI In Commercial Distribution 🇺🇸 United States

Kerlix

DI: 10884527023332 · Model: 7310 · Cardinal Health, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
10

Basic Information

Brand Name
Kerlix
Primary DI
10884527023332
Version / Model
7310
Catalog Number
7310
Company Name
Cardinal Health, Inc.
Labeler DUNS
080935429
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2018-06-30
Public Version
3
Public Version Date
2021-08-24
Public Version Status
Update
Public Device Record Key
87bbfe8a-61a0-4fbd-b970-d02681dc7217

Device Description

Super Sponges,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
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
48131 Non-woven gauze pad

Identifiers

Type ID
Package 20884527023339
Primary 10884527023332
Unit of Use 30884527023336

Customer Contacts

Device Sizes

Type Value Unit Text
Width 6 Inch
Length 6.75 Inch

Storage Conditions

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