FDA UDI Not in Commercial Distribution 🇺🇸 United States

Meijer One Step Pregnancy Test

DI: 00713733896320 · Model: FPPL · MEIJER, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Meijer One Step Pregnancy Test
Primary DI
00713733896320
Version / Model
FPPL
Company Name
MEIJER, INC.
Labeler DUNS
006959555
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-06-30
Public Version
5
Public Version Date
2023-07-06
Public Version Status
Update
Public Device Record Key
3dc65f92-6792-4bb4-8c3d-93ecc69bf8e1
Distribution End Date
2020-06-10

Device Description

FPPL Meijer SPS +/-

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 10713733896327
Primary 00713733896320

Customer Contacts

Phone
800-899-7353

Premarket Submissions

Submission Number Supplement Number
K042280 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
2 – 30 Degrees Celsius