FDA UDI In Commercial Distribution 🇺🇸 United States

Kroger

DI: 00041260012488 · Model: Advanced One Step +/- Pregnancy Test · KROGER CO., THE
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
2

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Basic Information

Brand Name
Kroger
Primary DI
00041260012488
Version / Model
Advanced One Step +/- Pregnancy Test
Company Name
KROGER CO., THE
Labeler DUNS
006999528
Distribution Status
In Commercial Distribution
Device Count in Pkg
2
Record Status
Published
Publish Date
2021-08-04
Public Version
4
Public Version Date
2024-02-06
Public Version Status
Update
Public Device Record Key
bee5c8a5-cf70-459a-b7f5-0366ed83a561

Device Description

Kroger DPS Advanced +/-

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
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
LCX Kit, Test, Pregnancy, Hcg, Over The Counter

GMDN Terms

Code Name
33819 Total human chorionic gonadotropin IVD, kit, rapid ICT, clinical

Identifiers

Type ID
Package 10041260012485
Primary 00041260012488
Unit of Use 00633472000492

Customer Contacts

Phone
800-632-6900

Premarket Submissions

Submission Number Supplement Number
K042280 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
2 – 30 Degrees Celsius