Homedics

GUDID 00031262102119

Neck Massager

ZHANGZHOU EASEPAL INNOVATION CO., LTD.

Hand-held electric massager

• Primary Device ID: 00031262102119
• NIH Device Record Key: 5b918b53-f628-4713-b727-4072e236eb25
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Homedics
• Version Model Number: NMSQ-216HJA-2
• Company DUNS: 546535934
• Company Name: ZHANGZHOU EASEPAL INNOVATION CO., LTD.
• 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	00006524176627 [Package]; Package: [4 Units]; In Commercial Distribution
GS1	00031262102119 [Primary]

FDA Product Code

• ISA: Massager, Therapeutic, Electric

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: 2025-03-10
• Device Publish Date: 2022-06-24

On-Brand Devices [Homedics]

• 00006524176610: Neck Massager
• 00031262102119: Neck Massager