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Nox A1® EEG 5 Lead Gold Electrode Cable

FDA UDI

Class II (US FDA UDI)

by Nox Medical ehf.

Identity

Trade Name
Nox A1® EEG 5 Lead Gold Electrode Cable FDA UDI
Generic Name
Analytical scalp electrode, reusable FDA UDI
Model / Reference
ECUP5AU1PAC1US FDA UDI

Identifiers

Catalog Number
554412 FDA UDI
Primary DI / UDI-DI
15694311111610 FDA UDI
510(k) Number
K192469 FDA UDI
FDA Product Code
OLZ FDA UDI
KZM FDA UDI
GMDN Term
Analytical scalp electrode, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.1400 FDA UDI
890.1375 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

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Analytical scalp electrode, reusable

Nox A1® EEG 5 Lead Gold Electrode Cable by Nox Medical ehf. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Analytical scalp electrode, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Nox Medical ehf.

Sources (1)

  • FDA UDI 90df20d2-49ef-4a8b-bd41-7ea2028744bf 35 fields · synced Jun 6, 2026