FDA UDI In Commercial Distribution 🇺🇸 United States

Kroger

DI: 00041260007804 · Model: AT 0270KRO · KROGER CO., THE
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Kroger
Primary DI
00041260007804
Version / Model
AT 0270KRO
Company Name
KROGER CO., THE
Labeler DUNS
006999528
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-06-11
Public Version
1
Public Version Date
2021-06-21
Public Version Status
New
Public Device Record Key
67a71ce5-268c-4e39-b537-7220c08da2ae

Device Description

Kroger Autolet Lancing Device

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
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
FMK Lancet, Blood

GMDN Terms

Code Name
37243 Manual blood lancing device, reusable

Identifiers

Type ID
Package 20041260007808
Primary 00041260007804
Package 10041260007801