FDA UDI Not in Commercial Distribution 🇺🇸 United States

Up & Up

DI: 00492450308636 · Model: One Step Ovulation Predictor PLUS Early Result Pregnancy Test · TARGET CORPORATION
Product Codes
2
GMDN Terms
2
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Up & Up
Primary DI
00492450308636
Version / Model
One Step Ovulation Predictor PLUS Early Result Pregnancy Test
Company Name
TARGET CORPORATION
Labeler DUNS
006961700
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-02-12
Public Version
8
Public Version Date
2023-12-18
Public Version Status
Update
Public Device Record Key
52c8b7ff-53b6-4cc5-91ec-3f90c3d97276
Distribution End Date
2020-07-17

Device Description

A convenience kit consisting of 7 up&up One Step Ovulation Predictor Tests + 1 up&up Early Result Pregnancy Test

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
Yes
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
CEP Radioimmunoassay, Luteinizing Hormone

GMDN Terms

Code Name
33819 Total human chorionic gonadotropin IVD, kit, rapid ICT, clinical
60862 Natural conception assistance kit

Identifiers

Type ID
Package 10492450308633
Primary 00492450308636

Customer Contacts

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
2 – 30 Degrees Celsius