Omniwave™ 042.001

GUDID 00860014139901

Omniwave is an electrically powered device intended for medical purposes, such as to relieve minor muscle aches and pains. Indications of use of Omniwave is intended for: Relief of minor muscle aches and pains; Temporary increase in local blood circulation; Activation of connective tissue.

Global Good, Corp.

Freestanding electric massager

• Primary Device ID: 00860014139901
• NIH Device Record Key: ff5e2072-e416-4f23-9140-2a25fefc1aaa
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Omniwave™
• Version Model Number: Quasoniq™
• Catalog Number: 042.001
• Company DUNS: 114420189
• Company Name: Global Good, Corp.
• Device Count: 1
• DM Exempt: true
• 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: true
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00860014139901 [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: 2025-06-25
• Device Publish Date: 2025-06-17