FDA UDI In Commercial Distribution 🇺🇸 United States

NuFACE

DI: 00850019720662 · Model: 42015 · Nuface
Product Codes
2
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NuFACE
Primary DI
00850019720662
Version / Model
42015
Company Name
Nuface
Labeler DUNS
023980008
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-06-08
Public Version
1
Public Version Date
2023-06-16
Public Version Status
New
Public Device Record Key
570bd043-7c29-4248-bb7e-7d7e0822d29e

Device Description

Trinity+ w/TWR+ Kit

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
Yes
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
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
OHS Light Based Over The Counter Wrinkle Reduction
NFO Stimulator, Transcutaneous Electrical, Aesthetic Purposes

GMDN Terms

Code Name
47704 Cosmetic red-light phototherapy system, home-use
46573 Physical therapy transcutaneous neuromuscular electrical stimulation system

Identifiers

Type ID
Primary 00850019720662

Premarket Submissions

Submission Number Supplement Number
K201782 000
K212947 000