FDA UDI In Commercial Distribution 🇺🇸 United States

Kerlix

DI: 20192253047278 · Model: 7310 · Cardinal Health 200, LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
10

Basic Information

Brand Name
Kerlix
Primary DI
20192253047278
Version / Model
7310
Catalog Number
7310-
Company Name
Cardinal Health 200, LLC
Labeler DUNS
961027315
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2024-07-23
Public Version
2
Public Version Date
2024-11-07
Public Version Status
Update
Public Device Record Key
90d1942f-d086-4937-b5c9-c835c3566a7a

Device Description

Kerlix Super Sponges

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 50192253047279
Primary 20192253047278
Unit of Use 10192253047271

Device Sizes

Type Value Unit Text
Width 6 Inch
Length 6.75 Inch