Identity
- Trade Name
- Johari Digital Healthcare Ltd. FDA UDI
- Generic Name
- Physical therapy transcutaneous neuromuscular electrical stimulation system FDA UDI
- Device Name
- 600 is the latest True Microcurrent machine designed for professional use. Delivering true intensity ranging from 175 to 600 micro amps, this machine ignites the ATP stimulation and sets a standard for non-invasive technology and the ability to provide long-lasting, natural facial lifting and toning results. This powerful True Microcurrent machine is only for licensed cosmetologists, aesthetics, or acupuncturists. This microcurrent machine for professionals is a perfect tool for boosting ATP for anti-aging, cellular repair, muscle re-education, skin firmness and tightening. FDA UDI
- Model / Reference
- Myolift 600 FDA UDI
- Description
- 600 is the latest True Microcurrent machine designed for professional use. Delivering true intensity ranging from 175 to 600 micro amps, this machine ignites the ATP stimulation and sets a standard for non-invasive technology and the ability to provide long-lasting, natural facial lifting and toning results. This powerful True Microcurrent machine is only for licensed cosmetologists, aesthetics, or acupuncturists. This microcurrent machine for professionals is a perfect tool for boosting ATP for anti-aging, cellular repair, muscle re-education, skin firmness and tightening. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08908008085376 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 25525fdc-dd0f-4b4f-9c68-f3cfc8a8dd2d 35 fields · synced May 30, 2026