FDA UDI In Commercial Distribution 🇺🇸 United States

Kroger

DI: 00041260383823 · Model: 041260383823 · KROGER CO., THE
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
10

Basic Information

Brand Name
Kroger
Primary DI
00041260383823
Version / Model
041260383823
Company Name
KROGER CO., THE
Labeler DUNS
006999528
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2019-08-30
Public Version
2
Public Version Date
2021-08-24
Public Version Status
Update
Public Device Record Key
2e40430d-ae64-4e17-a3af-d5935be6ee67

Device Description

Small Gauze Pads, all one size, 2 IN x 2 IN

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
Yes
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 10041260383820
Primary 00041260383823
Unit of Use 60041260383825