FDA UDI In Commercial Distribution 🇺🇸 United States

Johari Digital Healthcare Ltd.

DI: 08908008085369 · Model: Myolift QT · JOHARI DIGITAL HEALTHCARE LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Johari Digital Healthcare Ltd.
Primary DI
08908008085369
Version / Model
Myolift QT
Company Name
JOHARI DIGITAL HEALTHCARE LIMITED
Labeler DUNS
675938472
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-10-02
Public Version
3
Public Version Date
2023-06-02
Public Version Status
Update
Public Device Record Key
cc81fccd-89a1-45dc-82c3-916443e1bc0f

Device Description

MYOLIFT QT is a device based on true micro-current technology and one of the most advanced personal facial toning devices on the market. Its gentle, non-invasive electrical impulses are evenly channelled to the facial muscles through two applicator probes, re-educating & strengthening the muscle. MYOLIFT QT is portable device powered from the built-in battery or external power supply. The battery charger which is the integral part of device provides the fast and effective charging process. MYOLIFT QT is a portable device with Blue-Tooth (BT) connectivity with simple user- interface where the full control of device is provided through BT. Some simple actions and major indications can be achieved by using the interfaces which are built-in in device

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
No
PM Exempt
No
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
NFO Stimulator, Transcutaneous Electrical, Aesthetic Purposes

GMDN Terms

Code Name
46573 Physical therapy transcutaneous neuromuscular electrical stimulation system

Identifiers

Type ID
Primary 08908008085369

Customer Contacts

Phone
982-805-4228

Premarket Submissions

Submission Number Supplement Number
K112351 000