FDA UDI In Commercial Distribution 🇺🇸 United States

ELITONE

DI: 00851096008032 · Model: EE-1011 · ELIDAH, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
5

Basic Information

Brand Name
ELITONE
Primary DI
00851096008032
Version / Model
EE-1011
Company Name
ELIDAH, INC.
Labeler DUNS
079300140
Distribution Status
In Commercial Distribution
Device Count in Pkg
5
Record Status
Published
Publish Date
2021-04-08
Public Version
1
Public Version Date
2021-04-16
Public Version Status
New
Public Device Record Key
c5425c71-00e3-44a2-9299-f8e1835b50de

Device Description

ELITONE GelPads are transcutaneous electrodes to be used with the ELITONE Device.

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
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
QAJ Cutaneous Electrode Stimulator For Urinary Incontinence

GMDN Terms

Code Name
65017 Transcutaneous incontinence-control electrical stimulator electrode pad

Identifiers

Type ID
Unit of Use 00851096008025
Primary 00851096008032

Customer Contacts

Phone
978-435-4324

Premarket Submissions

Submission Number Supplement Number
K183585 000