Identity
- Trade Name
- Johari Digital Healthcare Ltd. FDA UDI
- Generic Name
- Physical therapy transcutaneous neuromuscular electrical stimulation system FDA UDI
- Device Name
- 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 FDA UDI
- Model / Reference
- Myolift QT FDA UDI
- 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 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08908008085369 FDA UDI
- 510(k) Number
- K112351 FDA UDI
- FDA Product Code
- NFO FDA UDI
- GMDN Term
- Physical therapy transcutaneous neuromuscular electrical stimulation system FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.5890 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Physical therapy transcutaneous neuromuscular electrical stimulation system
Johari Digital Healthcare Ltd. by Syrma Johari Medtech Limited — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Syrma Johari Medtech Limited
Sources (1)
- FDA UDI cc81fccd-89a1-45dc-82c3-916443e1bc0f 35 fields · synced May 31, 2026