Alpha-Stim SCS

GUDID 00857869005208

Alpha-Stim SCS kit

Electromedical Products International, Inc.

Psychiatric-therapy periauricular nerve transcutaneous electrical stimulator Psychiatric/stress-therapy periauricular nerve transcutaneous electrical stimulation system Psychiatric/stress-therapy periauricular nerve transcutaneous electrical stimulation system Psychiatric/stress-therapy periauricular nerve transcutaneous electrical stimulation system Psychiatric/stress-therapy periauricular nerve transcutaneous electrical stimulation system Psychiatric/stress-therapy periauricular nerve transcutaneous electrical stimulation system Psychiatric/stress-therapy periauricular nerve transcutaneous electrical stimulation system Psychiatric/stress-therapy periauricular nerve transcutaneous electrical stimulation system Psychiatric/stress-therapy periauricular nerve transcutaneous electrical stimulation system Psychiatric/stress-therapy periauricular nerve transcutaneous electrical stimulation system Psychiatric/stress-therapy periauricular nerve transcutaneous electrical stimulation system Psychiatric/stress-therapy periauricular nerve transcutaneous electrical stimulation system Psychiatric/stress-therapy periauricular nerve transcutaneous electrical stimulation system Psychiatric/stress-therapy periauricular nerve transcutaneous electrical stimulation system Psychiatric/stress-therapy periauricular nerve transcutaneous electrical stimulation system Psychiatric/stress-therapy periauricular nerve transcutaneous electrical stimulation system Psychiatric/stress-therapy periauricular nerve transcutaneous electrical stimulation system

• Primary Device ID: 00857869005208
• NIH Device Record Key: 05df7385-f8b6-4363-987b-75b98de40250
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Alpha-Stim SCS
• Version Model Number: SCS
• Company DUNS: 610954729
• Company Name: Electromedical Products International, Inc.
• 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: true
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: true
• 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	00857869005208 [Primary]

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2020-03-05
• Device Publish Date: 2014-10-28

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