Identity
- Trade Name
- IF-4 MultiWave FDA UDI
- Generic Name
- Physical therapy transcutaneous neuromuscular electrical stimulation system FDA UDI
- Device Name
- EMS stands for Electrical Neuromuscular Stimulator. The IF-4 MultiWave EMS system is indicated for: • Relaxation of muscle spasm; • Increasing local blood circulation and muscle re-education; • Prevention or retardation of disuse atrophy; • Prevention of venous thrombosis of the calf muscles immediately after surgery; • Maintaining or increasing range of motion. IF stands for Interferential Stimulation. The IF-4 MultiWave IF system is indicated for: • Symptomatic relief of chronic intractable pain. FDA UDI
- Model / Reference
- IF-4 MultiWave FDA UDI
- Description
- EMS stands for Electrical Neuromuscular Stimulator. The IF-4 MultiWave EMS system is indicated for: • Relaxation of muscle spasm; • Increasing local blood circulation and muscle re-education; • Prevention or retardation of disuse atrophy; • Prevention of venous thrombosis of the calf muscles immediately after surgery; • Maintaining or increasing range of motion. IF stands for Interferential Stimulation. The IF-4 MultiWave IF system is indicated for: • Symptomatic relief of chronic intractable pain. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 06942808291478 FDA UDI
- FDA Product Code
- IPF FDA UDILIH FDA UDI
- GMDN Term
- Physical therapy transcutaneous neuromuscular electrical stimulation system FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 890.5850 FDA UDI882.5890 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
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Physical therapy transcutaneous neuromuscular electrical stimulation system
IF-4 MultiWave by EasyMed Instruments Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- EasyMed Instruments Co., Ltd.
Sources (1)
- FDA UDI 45515b63-0550-4ca9-b588-52387eec807d 33 fields · synced Jun 8, 2026