Etekcity Neck Massager Heated Pro

GUDID 00817915020241

Etekcity Neck Massager Heated Pro

ETEKCITY CORPORATION

Wearable electric massager

• Primary Device ID: 00817915020241
• NIH Device Record Key: 7ea7ede1-a167-4382-aea4-547586ff4a1d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Etekcity Neck Massager Heated Pro
• Version Model Number: ENM-C221-AUS
• Company DUNS: 079578783
• Company Name: ETEKCITY CORPORATION
• 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: false
• 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00817915020241 [Primary]
GS1	10817915020248 [Package]; Package: Outer Carton [4 Units]; In Commercial Distribution

FDA Product Code

• ISA: Massager, Therapeutic, Electric

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: 2025-04-08
• Device Publish Date: 2025-03-31

On-Brand Devices [Etekcity Neck Massager Heated Pro]

• 10817915020255: Etekcity Neck Massager Heated Pro
• 00817915020241: Etekcity Neck Massager Heated Pro