aireeg

FDA UDI

Class II (US FDA UDI)

by Nihon Kohden Corp.

Identity

Trade Name: aireeg FDA UDI
Generic Name: Electroencephalograph FDA UDI
Device Name: Main unit for WEE-1200 FDA UDI
Model / Reference: MU-120A FDA UDI
Description: Main unit for WEE-1200 FDA UDI

Identifiers

Catalog Number: MU-120A FDA UDI
Primary DI / UDI-DI: 04931921130469 FDA UDI
FDA Product Code: OLV FDA UDI
GWQ FDA UDI
GMDN Term: Electroencephalograph FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 882.1400 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

MRI Safety

MR Unsafe FDA UDI

Category: Electroencephalograph

aireeg by Nihon Kohden Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Natus — Natus Neurology Incorporated · Class II
128-channel EEG cap (L) — Megin Oy · Class II
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Zeto ONE Head Unit - Small — ZETO INC · 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: Nihon Kohden Corp.

Sources (1)

FDA UDI b4fb1e1b-b0e2-4307-99e5-ebc2f003d14e 35 fields · synced Jun 8, 2026