FDA UDI In Commercial Distribution 🇺🇸 United States

iProven

DI: 08719699633230 · Model: FMH-139-5 · Sevenground Trading B.V.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
5

Basic Information

Brand Name
iProven
Primary DI
08719699633230
Version / Model
FMH-139-5
Company Name
Sevenground Trading B.V.
Labeler DUNS
492177197
Distribution Status
In Commercial Distribution
Device Count in Pkg
5
Record Status
Published
Publish Date
2019-06-04
Public Version
2
Public Version Date
2023-07-06
Public Version Status
Update
Public Device Record Key
7b865cab-87fc-47c7-aba5-35d2f7654284

Device Description

FMH-139 is a One Step HCG Urine Pregnancy Test

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
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
Yes
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

GMDN Terms

Code Name
33819 Total human chorionic gonadotropin IVD, kit, rapid ICT, clinical

Identifiers

Type ID
Primary 08719699633230
Unit of Use 08719699633636

Customer Contacts

Phone
18555178225