FDA UDI In Commercial Distribution 🇺🇸 United States

HORMONElife™

DI: 00816862027242 · Model: W52-S-SQ-6BX · WONDFO USA CO., LTD.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
6

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
HORMONElife™
Primary DI
00816862027242
Version / Model
W52-S-SQ-6BX
Company Name
WONDFO USA CO., LTD.
Labeler DUNS
849098897
Distribution Status
In Commercial Distribution
Device Count in Pkg
6
Record Status
Published
Publish Date
2025-07-03
Public Version
1
Public Version Date
2025-07-11
Public Version Status
New
Public Device Record Key
356154ba-16c6-4790-bdc5-1be0853026d8

Device Description

HORMONElife™ Ultra Accurate FSH Test Strip OTC 6PK

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
Yes
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
NGA Test, Follicle Stimulating Hormone (Fsh), Over The Counter

GMDN Terms

Code Name
65841 Follicle stimulating hormone (FSH) IVD, kit, rapid ICT, self-testing

Identifiers

Type ID
Package 10816862027249
Primary 00816862027242
Unit of Use 00816862027235

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
4 – 30 Degrees Celsius