Alpha-Stim Earclip Electrode (M)

GUDID 00857869005161

Alpha-Stim Earclip Electrode (M) RoHS compliant

Electromedical Products International, Inc.

Transcutaneous electrical stimulation electrode 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: 00857869005161
• NIH Device Record Key: ebf63866-9263-462e-aa49-4d08034fed13
• Commercial Distribution Discontinuation: 2014-08-29
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Alpha-Stim Earclip Electrode (M)
• Version Model Number: Earclip Electrode (M) [RoHS]
• Company DUNS: 610954729
• Company Name: Electromedical Products International, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00857869005161 [Primary]

FDA Product Code

• JXK: Stimulator, Cranial Electrotherapy

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2014-08-29

On-Brand Devices [Alpha-Stim Earclip Electrode (M)]

• 00857869005161: Alpha-Stim Earclip Electrode (M) RoHS compliant
• 00857869005147: Alpha-Stim Earclip Electrode (M)