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Nihon Kohden, EEG-1200A Series Neurofax

FDA UDI

Class II (US FDA UDI)

by Nihon Kohden Corp.

Identity

Trade Name
Nihon Kohden, EEG-1200A Series Neurofax FDA UDI
Generic Name
Instrument trolley FDA UDI
Device Name
Cart, used with EEG-1200A, works with standard and optional accessories FDA UDI
Model / Reference
KD-029A-01 FDA UDI
Description
Cart, used with EEG-1200A, works with standard and optional accessories FDA UDI

Identifiers

Catalog Number
KD-029A-01 FDA UDI
Primary DI / UDI-DI
04931921007723 FDA UDI
FDA Product Code
OLT FDA UDI
GMDN Term
Instrument trolley 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

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Instrument trolley

Nihon Kohden, EEG-1200A Series Neurofax by Nihon Kohden Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Instrument trolley.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Nihon Kohden Corp.

Sources (1)

  • FDA UDI 309ad017-5f9d-4c4f-9d6d-b4f592908969 35 fields · synced May 30, 2026