FDA UDI In Commercial Distribution 🇺🇸 United States

Vivoo

DI: 00860015215826 · Model: VWHL25V1 · VIVOSENS INC.
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
70

Basic Information

Brand Name
Vivoo
Primary DI
00860015215826
Version / Model
VWHL25V1
Company Name
VIVOSENS INC.
Labeler DUNS
086601609
Distribution Status
In Commercial Distribution
Device Count in Pkg
70
Record Status
Published
Publish Date
2026-01-19
Public Version
1
Public Version Date
2026-01-27
Public Version Status
New
Public Device Record Key
7eb547aa-c431-476a-b78b-91097f1c0990

Device Description

20-Strips HCG Pregnancy Tests, 50-Strips LH-Ovulation Test, and 70 Plastic Urine Cups

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
No
Has Manufacturing Date
No
Has Expiration Date
No
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 20860011489164
Primary 00860015215826

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
2 – 30 Degrees Celsius