FDA UDI In Commercial Distribution 🇺🇸 United States

HORMONElife™

DI: 10810174471059 · Model: DWS-H10L20-H · WONDFO USA CO., LTD.
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
30

Basic Information

Brand Name
HORMONElife™
Primary DI
10810174471059
Version / Model
DWS-H10L20-H
Company Name
WONDFO USA CO., LTD.
Labeler DUNS
849098897
Distribution Status
In Commercial Distribution
Device Count in Pkg
30
Record Status
Published
Publish Date
2025-12-05
Public Version
1
Public Version Date
2025-12-15
Public Version Status
New
Public Device Record Key
a65a3cff-fd38-4c82-8c96-4c6f5afbddae

Device Description

HORMONELife 10+20 Strip Combo; 10 hCG Pregnancy Test + 20 LH Ovulation

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
No
Combination Product
Yes
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
NGE Test, Luteinizing Hormone (Lh), Over The Counter

GMDN Terms

Code Name
60862 Natural conception assistance kit

Identifiers

Type ID
Unit of Use 00810174471052
Primary 10810174471059

Customer Contacts

Phone
630-468-2199