Identity
- Trade Name
- CHATTANOOGA FDA UDI
- Generic Name
- Electromyography monitor FDA UDI
- Device Name
- EMG MODULE PKG FDA UDI
- Model / Reference
- 2799 FDA UDI
- Description
- EMG MODULE PKG FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00888912294829 FDA UDI
- FDA Product Code
- HCC FDA UDI
- GMDN Term
- Electromyography monitor FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.5050 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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Electromyography monitor
Chattanooga by Djo, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Electromyography monitor.
- PMRU-S KIT — EMERGE DIAGNOSTICS LLC · Class II
- CHATTANOOGA — DJO, LLC · Class II
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
- Djo, Llc
Sources (1)
- FDA UDI d4fddfd4-3305-4db6-87b6-4bf46ec2da17 33 fields · synced May 29, 2026