Identity
- Trade Name
- PMRU-S KIT FDA UDI
- Generic Name
- Electromyography monitor FDA UDI
- Device Name
- Electrical diagnostic functional assessment, combining range of motion, functional capacity, and electromyography testing FDA UDI
- Model / Reference
- 7200 FDA UDI
- Description
- Electrical diagnostic functional assessment, combining range of motion, functional capacity, and electromyography testing FDA UDI
Identifiers
- Primary DI / UDI-DI
- B25972000 FDA UDI
- 510(k) Number
- K123902 FDA UDI
- FDA Product Code
- OAL FDA UDI
- GMDN Term
- Electromyography monitor FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 890.1375 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
No
FDA UDI
Category: Electromyography monitor
Pmru-S Kit by Emerge Diagnostics Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Electromyography monitor.
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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
- Emerge Diagnostics Llc
Sources (1)
- FDA UDI dc44d308-3794-4415-b2b1-6abcbdb4db13 34 fields · synced Jun 8, 2026