Primary Device ID | 00879314000026 |
NIH Device Record Key | d45049c8-6124-4f23-a0f4-d016a3743aa7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | FaceMaster |
Version Model Number | Platinum |
Catalog Number | 700015-A |
Company DUNS | 014107160 |
Company Name | FACEMASTER OF BEVERLY HILLS, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
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 | 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 Issuing Agency | Device ID |
---|---|
GS1 | 00879314000026 [Primary] |
NFO | Stimulator, Transcutaneous Electrical, Aesthetic Purposes |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2019-10-23 |
Device Publish Date | 2018-12-31 |
00879314000033 | Reconditioned and recycled FaceMaster Platinum Facial Toning System |
00879314000026 | FaceMaster Platinum Facial Toning System |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
FACEMASTER 75741052 not registered Dead/Abandoned |
Aesthetic Innovations, Inc. 1999-07-01 |
FACEMASTER 75133823 2298448 Live/Registered |
Facemaster Of Beverly Hills, Inc. 1996-07-15 |