Identity
- Trade Name
- Neuromaster FDA UDI
- Generic Name
- Neurophysiologic monitoring system FDA UDI
- Device Name
- Main unit for MEE-1000A FDA UDI
- Model / Reference
- DC-110BA FDA UDI
- Description
- Main unit for MEE-1000A FDA UDI
Identifiers
- Catalog Number
- DC-110BA FDA UDI
- Primary DI / UDI-DI
- 04931921102152 FDA UDI
- FDA Product Code
- GWF FDA UDI
- GMDN Term
- Neurophysiologic monitoring system FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.1870 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
No
FDA UDI
MR Unsafe FDA UDI
Category: Neurophysiologic monitoring system
Neuromaster by Nihon Kohden Corp. — 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
- Nihon Kohden Corp.
Sources (1)
- FDA UDI cef0b5ec-83b5-4c35-a74b-00ae52090536 35 fields · synced May 30, 2026