FDA UDI In Commercial Distribution 🇺🇸 United States

FaceMaster

DI: 00879314000033 · Model: Platinum · FACEMASTER OF BEVERLY HILLS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
FaceMaster
Primary DI
00879314000033
Version / Model
Platinum
Catalog Number
700016-A
Company Name
FACEMASTER OF BEVERLY HILLS, INC.
Labeler DUNS
014107160
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-12-31
Public Version
8
Public Version Date
2023-06-02
Public Version Status
Update
Public Device Record Key
8a39278d-b0ec-445a-888a-f64b2f191b80

Device Description

Reconditioned and recycled FaceMaster Platinum Facial Toning System

Device Characteristics

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

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
NFO Stimulator, Transcutaneous Electrical, Aesthetic Purposes

GMDN Terms

Code Name
46573 Physical therapy transcutaneous neuromuscular electrical stimulation system

Identifiers

Type ID
Primary 00879314000033

Customer Contacts

Phone
8007702521