FDA UDI In Commercial Distribution 🇺🇸 United States

Kerlix

DI: 10192253050288 · Model: 5360 · Cardinal Health 200, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Kerlix
Primary DI
10192253050288
Version / Model
5360
Catalog Number
5360-
Company Name
Cardinal Health 200, LLC
Labeler DUNS
961027315
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-03-24
Public Version
1
Public Version Date
2023-04-03
Public Version Status
New
Public Device Record Key
e014120c-f473-4dbd-8d31-9adbe453c053

Device Description

5360 PACKING SPG STR-1'S

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
GDY Gauze/sponge, internal, x-ray detectable

GMDN Terms

Code Name
38496 Radiopaque woven surgical sponge

Identifiers

Type ID
Package 50192253050286
Primary 10192253050288