Neuromaster DC-110BA

by Nihon Kohden Corporation

Neuromaster DC-110BA is a Class II device made by Nihon Kohden Corporation, listed in FDA GUDID since 5 Sep 2016 (UDI-DI 04931921102152), registry data as of 12 Nov 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Source GUDID, synced 12 Nov 2026.

Regulatory status

as of registry sync 12 Nov 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number04931921102152 UDI-DI	Date5 Sep 2016Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 04931921102152

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Neuromaster
Generic name: Neurophysiologic monitoring system
Model / Ref / Catalog: DC-110BA

Primary DI / UDI-DI: 04931921102152
FDA product code: GWF
GMDN term: Neurophysiologic monitoring system

Device class: Class II
Regulation number: 882.1870
GUDID distribution status: In Commercial Distribution

MRI safety: MR Unsafe

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Properties

Prescription use
Serial number

Other properties (13, all answered No)