FDA UDI In Commercial Distribution 🇺🇸 United States

Omniwave™

DI: 00860014139901 · Model: Quasoniq™ · Global Good, Corp.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Omniwave™
Primary DI
00860014139901
Version / Model
Quasoniq™
Catalog Number
042.001
Company Name
Global Good, Corp.
Labeler DUNS
114420189
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-06-17
Public Version
1
Public Version Date
2025-06-25
Public Version Status
New
Public Device Record Key
ff5e2072-e416-4f23-9140-2a25fefc1aaa

Device Description

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.

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
Yes
PM Exempt
Yes
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
ISA Massager, Therapeutic, Electric

GMDN Terms

Code Name
35538 Freestanding electric massager

Identifiers

Type ID
Primary 00860014139901