Device
3 pairs of reusable gel pads
Manufacturer
PAIN MANAGEMENT TECHNOLOGIES, INC.
Model: Long gel pads DI: 00855569006211 Status: New MRI: Labeling does not contain MRI Safety Information Single-use: No Rx: No OTC: Yes
First Published: 2026-05-04 Current Version: 2026-05-12
Description
3 pairs of reusable gel pads
Sterilization
Device Sterile: No
Sterilization Prior To Use: No
Regulatory & Distribution
Record Status: Published
Version Number: 1
Record Key: 1b072158-7584-4e31-895e-8e48e760b96c
Distribution Status: In Commercial Distribution
DUNS Number: 617940346
Device Count: 1
DM Exempt: No
Premarket Exempt: No
HCT/P: No
Kit: No
Combination Product: No
Lot/Batch Tracked: Yes
Serial Number Tracked: No
Manufacturing Date Tracked: No
Expiration Date Tracked: Yes
Donation ID Number Tracked: No
Labeled Contains NRL: No
Labeled No NRL: No
Identifiers
Item #1 - Pkg Type: Small Box
Item #1 - Device ID: 10855569006218
Item #1 - Pkg Status: In Commercial Distribution
Item #1 - Pkg Quantity: 3
Item #1 - Device ID Type: Package
Item #1 - Contains DINumber: 00855569006211
Item #1 - Device ID Issuing Agency: GS1
Item #2 - Device ID: 00855569006211
Item #2 - Device ID Type: Primary
Item #2 - Device ID Issuing Agency: GS1
Item #3 - Pkg Type: Carton box
Item #3 - Device ID: 20855569006215
Item #3 - Pkg Status: In Commercial Distribution
Item #3 - Pkg Quantity: 48
Item #3 - Device ID Type: Package
Item #3 - Contains DINumber: 10855569006218
Item #3 - Device ID Issuing Agency: GS1
GMDN
Code: 35995
Name: Transcutaneous electrical stimulation electrode, single-use
Definition:
An electrical conductor intended to be attached to a patient's skin (noninvasive) to provide therapeutic electrical stimuli through the body surface [e.g., transcutaneous electrical nerve stimulation (TENS), electrical muscle stimulation (EMS), cranial electrotherapy stimulation (CES)]. It is typically a flat, flexible, conductive pad with an adhesive (e.g., gel), or a preformed shape/mechanism designed for attachment to a particular body part (e.g., earclip), connected to a conductive wire. This is a single-use device.
FDA Product Codes
GXY
Electrode, Cutaneous
Premarket Submissions
Submission Number: K142099
Supplement Number: 000