FDA UDI In Commercial Distribution 🇺🇸 United States

Vivoo

DI: 00860011489153 · Model: VWHF25V1 · VIVOSENS INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
10

Basic Information

Brand Name
Vivoo
Primary DI
00860011489153
Version / Model
VWHF25V1
Company Name
VIVOSENS INC.
Labeler DUNS
086601609
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2024-11-25
Public Version
1
Public Version Date
2024-12-03
Public Version Status
New
Public Device Record Key
dfe5ca2a-806f-4487-ab3e-143afba3254d

Device Description

Vivoo FSH Fertility Test (Urine), with 10 products inside.

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
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
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 10860011489150
Primary 00860011489153
Unit of Use 20860011489157

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
2 – 30 Degrees Celsius