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Olympic CFM

FDA UDI

Class II (US FDA UDI)

by Natus Medical Incorporated

Identity

Trade Name
Olympic CFM FDA UDI
Generic Name
Analytical scalp electrode, single-use FDA UDI
Device Name
Neonatal EEG Hydrogel sensor FDA UDI
Model / Reference
Electrode Hydrogel FDA UDI
Description
Neonatal EEG Hydrogel sensor FDA UDI

Identifiers

Catalog Number
200249-507, 62050, 62051 FDA UDI
Primary DI / UDI-DI
00382830053839 FDA UDI
FDA Product Code
OMA FDA UDI
OMC FDA UDI
GMDN Term
Analytical scalp electrode, single-use 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

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Analytical scalp electrode, single-use

Olympic CFM by Natus Medical Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Analytical scalp electrode, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b751f9b8-407e-4c16-8091-aedba87725a4 35 fields · synced May 30, 2026