Homedics

GUDID 00031262114129

Cupping therapy Massager

Electrical Appliance Branch of Zhangzhou Easepal Industrial Corporation

Hand-held electric massager

• Primary Device ID: 00031262114129
• NIH Device Record Key: 69b52efe-c10c-4e10-8db5-e76204ca8ae5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Homedics
• Version Model Number: SPE-CP110HJ
• Company DUNS: 544372391
• Company Name: Electrical Appliance Branch of Zhangzhou Easepal Industrial 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: 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: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	00031262114129 [Primary]

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: 2024-07-12
• Device Publish Date: 2024-07-04

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• 00031262107213: Eye Massager
• 00031262109781: Neck Massager
• 00031262109309: Neck Massager
• 00031262109095: Neck Massager
• 00031262109064: Eye Massager
• 00031262108982: Neck Massager
• 00031262108807: Massage Roller Ball
• 00031262108609: Foot Massager
• 00031262110695: Foot Massager
• 00031262113085: Neck Massager
• 00031262112521: Foot Massager
• 00031262115348: Neck Massager
• 00031262113023: Neck Massager
• 00031262115522: Neck Massager
• 00031262114129: Cupping therapy Massager