FDA UDI In Commercial Distribution 🇺🇸 United States

Kerlix

DI: 10884521083417 · Model: 7884 · Cardinal Health, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
2

Basic Information

Brand Name
Kerlix
Primary DI
10884521083417
Version / Model
7884
Catalog Number
7884
Company Name
Cardinal Health, Inc.
Labeler DUNS
080935429
Distribution Status
In Commercial Distribution
Device Count in Pkg
2
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
487219b4-9f28-4518-8703-1fcae0bcb410

Device Description

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
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
48131 Non-woven gauze pad

Identifiers

Type ID
Package 20884521083414
Primary 10884521083417
Unit of Use 30884521083411

Customer Contacts

Device Sizes

Type Value Unit Text
Width 6 Inch
Length 6.75 Inch

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
;