Identity
- Trade Name
- Ibramed FDA UDI
- Generic Name
- Physical therapy ultrasound/neuromuscular stimulation system FDA UDI
- Device Name
- NEUROTONUS MULTIWAVE transcutaneous neuromuscular stimulator is a four-channel stimulator with independente controls for current therapies used in: TENS (Transcutaneous Electrical Nerve Stimulation), FES (Functional Electrical Stimulation); RUSSIAN CURRENT (Burst Modulated Medium Frequency), AUSSIE CURRENT (Burst Modulated Medium Frequency), INTERFERENTIAL CURRENT (Amplitude Modulated Medium Frequency), DIRECT CURRENT/POLARIZED CURRENT or MICROCURRENT. FDA UDI
- Model / Reference
- NEUROTONUS MULTIWAVE FDA UDI
- Description
- NEUROTONUS MULTIWAVE transcutaneous neuromuscular stimulator is a four-channel stimulator with independente controls for current therapies used in: TENS (Transcutaneous Electrical Nerve Stimulation), FES (Functional Electrical Stimulation); RUSSIAN CURRENT (Burst Modulated Medium Frequency), AUSSIE CURRENT (Burst Modulated Medium Frequency), INTERFERENTIAL CURRENT (Amplitude Modulated Medium Frequency), DIRECT CURRENT/POLARIZED CURRENT or MICROCURRENT. FDA UDI
Identifiers
- Catalog Number
- 01002023 FDA UDI
- Primary DI / UDI-DI
- 07898961579108 FDA UDI
- 510(k) Number
- K131629 FDA UDI
- FDA Product Code
- LIH FDA UDIIPF FDA UDIGZJ FDA UDIGZI FDA UDI
- GMDN Term
- Physical therapy ultrasound/neuromuscular stimulation system FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.5890 FDA UDI890.5850 FDA UDI882.5810 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
Yes
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
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Physical therapy ultrasound/neuromuscular stimulation system
Ibramed by Ibramed Industria Brasileira de Equipamentos Medicos Eir — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K131629 also covers:
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
Sources (1)
- FDA UDI 03f7633d-1255-4199-91e4-83fb15cb063d 35 fields · synced Jun 8, 2026