FDA UDI In Commercial Distribution 🇺🇸 United States

WELL-LIFE

DI: 04719872260073 · Model: SP-5181 · WELL-LIFE HEALTHCARE LTD.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
WELL-LIFE
Primary DI
04719872260073
Version / Model
SP-5181
Company Name
WELL-LIFE HEALTHCARE LTD.
Labeler DUNS
658608864
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-05-02
Public Version
5
Public Version Date
2020-10-19
Public Version Status
Update
Public Device Record Key
3d026ef8-2a03-4666-8c93-5d0c070b08b5

Device Description

The Well Life Self Adhesive Electrode / CM, FA, PU and SP series are intended for use as a disposable, conductive adhesive interface between the patient's skin and the Electrical Stimulator. Well Life Self Adhesive Electrode / CM, FA, PU and SP series are designed and intended to be used with marketed Electrical Stimulators, i.e. TENS, EMS, IF, and PGS.

Device Characteristics

Single Use
No
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
MR Safe
Direct Marking Exempt
Yes
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
LIH Interferential Current Therapy

GMDN Terms

Code Name
46571 Physical therapy transcutaneous electrical stimulation system, line-powered

Identifiers

Type ID
Primary 04719872260073