FDA UDI In Commercial Distribution 🇺🇸 United States

Kerlix

DI: 20192253046172 · Model: 4935 · Cardinal Health 200, LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
5

Basic Information

Brand Name
Kerlix
Primary DI
20192253046172
Version / Model
4935
Catalog Number
4935-
Company Name
Cardinal Health 200, LLC
Labeler DUNS
961027315
Distribution Status
In Commercial Distribution
Device Count in Pkg
5
Record Status
Published
Publish Date
2023-03-27
Public Version
1
Public Version Date
2023-04-04
Public Version Status
New
Public Device Record Key
55712625-836d-4979-89ce-32ecbd8e013b

Device Description

Kerlix X-Ray Detectable Round Sponges, X-Large

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
Yes
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
GDY Gauze/sponge, internal, x-ray detectable

GMDN Terms

Code Name
38496 Radiopaque woven surgical sponge

Identifiers

Type ID
Package 50192253046173
Primary 20192253046172
Unit of Use 10192253046175