FDA UDI In Commercial Distribution 🇺🇸 United States

Meijer

DI: 00760236195818 · Model: 20002291 · MEIJER, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
2

Basic Information

Brand Name
Meijer
Primary DI
00760236195818
Version / Model
20002291
Catalog Number
N/A
Company Name
MEIJER, INC.
Labeler DUNS
006959555
Distribution Status
In Commercial Distribution
Device Count in Pkg
2
Record Status
Published
Publish Date
2026-04-01
Public Version
1
Public Version Date
2026-04-09
Public Version Status
New
Public Device Record Key
5ebb4155-4e4e-488f-8f62-9f7880f0d3d5

Device Description

Meijer DPS 6 Day Blue

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 10760236195815
Primary 00760236195818
Unit of Use 00633472000683

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K213379 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
2 – 30 Degrees Celsius