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128-channel EEG cap (L)

FDA UDI

Class II (US FDA UDI)

by Megin Oy

Identity

Trade Name
128-channel EEG cap (L) FDA UDI
Generic Name
Electroencephalograph FDA UDI
Device Name
A non-magnetic 128-channel EEG cap (size 56-62 cm) with sintered Ag/AgCl electrodes. FDA UDI
Model / Reference
NM24393N FDA UDI
Description
A non-magnetic 128-channel EEG cap (size 56-62 cm) with sintered Ag/AgCl electrodes. FDA UDI

Identifiers

Catalog Number
NM23896N FDA UDI
Primary DI / UDI-DI
06430056480183 FDA UDI
FDA Product Code
OLY 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

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Category: Electroencephalograph

128-channel EEG cap (L) by Megin Oy — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electroencephalograph.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Megin Oy

Sources (1)

  • FDA UDI ee2e80a5-05ac-4ff2-9392-a7ee0fa4f710 34 fields · synced Jun 8, 2026