Three degrees

GUDID 06976378040006

Rectangular shape TENS/EMS Electrode Pads includes specification of 10*100, 15*40, 17*70, 20*40, 20*80, 20*100, 25*35, 30*50, 30*60, 30*70, 30*90, 32*95, 35*45, 35*50, 35*70, 35*82, 40*53, 40*60, 40*70, 40*90, 40*100, 45*60, 45*70, 45*90, 45*95, 46*73, 50*55, 50*60, 50*70, 50*80, 50*90, 50*100, 52*78, 53*210, 55*90, 50*96, 55*100, 60*70, 60*80, 60*90, 60*100, 62*96, 65*140, 68*88, 70*70, 70*100, 70*110, 70*130, 70*140, 73*160, 90*130, 95*100, 95*195, 96*162, 98*220, 100*150, 110*150, 115*180, 150*200.

Dong Guan Ou Kang Electronics CO.,LTD

Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use Transcutaneous electrical stimulation electrode, single-use

• Primary Device ID: 06976378040006
• NIH Device Record Key: 133247bf-e895-4586-8d21-46c3de145791
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Three degrees
• Version Model Number: Rectangular
• Company DUNS: 554408363
• Company Name: Dong Guan Ou Kang Electronics CO.,LTD
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	06976378040006 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K181234

FDA Product Code

• GXY: Electrode, Cutaneous

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-08-16
• Device Publish Date: 2023-08-08

On-Brand Devices [Three degrees]

• 06976378040044: Hand shape TENS/EMS Electrode Pads includes specification of 25*50, 46*75, 50*78, 55*80, 64*78,
• 06976378040037: Oval shape TENS/EMS Electrode Pads includes specification of 15*60, 30*43, 30*50, 40*60, 42*67,
• 06976378040020: Circular shape TENS/EMS Electrode Pads includes specification of Φ15, Φ20, Φ22, Φ25, Φ30, �
• 06976378040013: Square shape TENS/EMS Electrode Pads includes specification of 20*20, 30*30, 40*40, 50*50, 6
• 06976378040006: Rectangular shape TENS/EMS Electrode Pads includes specification of 10*100, 15*40, 17*70, 20*40,