Painmaster

GUDID 20781604000125

Transcutaneous electrical stimulation electrode

Primary Device ID	20781604000125
NIH Device Record Key	620a285d-8b9f-479b-95ef-44c1f1580f18
Commercial Distribution Status	In Commercial Distribution
Brand Name	Painmaster
Version Model Number	Women's Oval Snap Tens Electrode
Company DUNS	003775302
Company Name	Painmaster
Device Count	1
DM Exempt	false
Pre-market Exempt	false
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	false
Lot Batch	true
Serial Number	true
Manufacturing Date	true
Expiration Date	true
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	true
RX Perscription	true
OTC Over-The-Counter	true

Device Issuing Agency	Device ID
GS1	00781604000121 [Primary]
GS1	10781604000128 [Package] Contains: 00781604000121 Package: Inner Box/Pack [2 Units] In Commercial Distribution
GS1	20781604000125 [Package] Contains: 10781604000128 Package: Master Case [40 Units] In Commercial Distribution

GXY	Electrode, Cutaneous

Steralize Prior To Use	false
Device Is Sterile	false

20781604000132	Bell Shaped Snap Tens Electrode- 20x90mm in Size
20781604000125	Women's Oval Snap Tens Electrode - 40x90mm in Size

Mark Image Registration \| Serial	Company Trademark Application Date
PAINMASTER 78247258 2823528 Live/Registered	NEWMARK, INC. 2003-05-08
PAINMASTER 74561861 1945234 Dead/Cancelled	REIMERS & JANSSEN GMBH MEDIZINTECHNIK 1994-08-15