FDA UDI In Commercial Distribution 🇺🇸 United States

Elitone URGE

DI: 00851096008117 · Model: EK-1019 · Elidah, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Elitone URGE
Primary DI
00851096008117
Version / Model
EK-1019
Company Name
Elidah, Inc.
Labeler DUNS
079300140
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-12-19
Public Version
2
Public Version Date
2025-11-20
Public Version Status
Update
Public Device Record Key
a1636e51-ebf5-4926-b5b0-e82c118c9710

Device Description

Elitone URGE Therapy Kit, includes 1x Elitone URGE (00851096008100) and 2x Elitone GelPad packs (00851096008032)

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
Yes
Kit
Yes
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
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
QAJ Cutaneous Electrode Stimulator For Urinary Incontinence

GMDN Terms

Code Name
65016 Transcutaneous incontinence-control electrical stimulator

Identifiers

Type ID
Primary 00851096008117