Easy@Home Electronic Pain Relief Stimulator

GUDID 10810038634002

EASY HEALTHCARE CORPORATION

Pain-relief static magnet Pain-relief static magnet Pain-relief static magnet Pain-relief static magnet Pain-relief static magnet Pain-relief static magnet Pain-relief static magnet Pain-relief static magnet Pain-relief static magnet Pain-relief static magnet Pain-relief static magnet Pain-relief static magnet Static magnetic therapeutic clothing/jewelry Static magnetic therapeutic clothing/jewelry Static magnetic therapeutic clothing/jewelry Static magnetic therapeutic clothing/jewelry Static magnetic therapeutic clothing/jewelry Static magnetic therapeutic clothing/jewelry Static magnetic therapeutic clothing/jewelry Static magnetic therapeutic clothing/jewelry Static magnetic therapeutic clothing/jewelry Static magnetic therapeutic clothing/jewelry Static magnetic therapeutic clothing/jewelry Static magnetic therapeutic clothing/jewelry Static magnetic therapeutic clothing/jewelry Static magnetic therapeutic clothing/jewelry Static magnetic therapeutic clothing/jewelry

• Primary Device ID: 10810038634002
• NIH Device Record Key: 39336fbc-5b0e-4d90-9377-b70f58f318bb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Easy@Home Electronic Pain Relief Stimulator
• Version Model Number: EHE019
• Company DUNS: 080278407
• Company Name: EASY HEALTHCARE CORPORATION
• 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: false
• Manufacturing Date: true
• 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: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	00810038634005 [Primary]
GS1	10810038634002 [Package]; Contains: 00810038634005; Package: [80 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K153520

FDA Product Code

• NUH: Stimulator, Nerve, Transcutaneous, Over-The-Counter

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: 2022-10-10
• Device Publish Date: 2022-09-30

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