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EVO sEEG Electrode

FDA UDI

Class II (US FDA UDI)

by Neuroone Medical Technologies Corp.

Identity

Trade Name
EVO sEEG Electrode FDA UDI
Generic Name
Percutaneous radio-frequency ablation probe, brain-ablation FDA UDI
Device Name
26.5mm x 8 Contact sEEG - RF Probe FDA UDI
Model / Reference
NSEEG2708-RF FDA UDI
Description
26.5mm x 8 Contact sEEG - RF Probe FDA UDI

Identifiers

Primary DI / UDI-DI
00856895008580 FDA UDI
FDA Product Code
GXI FDA UDI
GZL FDA UDI
GMDN Term
Percutaneous radio-frequency ablation probe, brain-ablation FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4725 FDA UDI
882.1330 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Depth electrodePercutaneous radio-frequency ablation probe, brain-ablation

EVO sEEG Electrode by Neuroone Medical Technologies Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Percutaneous radio-frequency ablation probe, brain-ablation.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Neuroone Medical Technologies Corp.

Sources (1)

  • FDA UDI 795a9a94-13e3-4fad-8cff-af44a2842a9e 33 fields · synced May 30, 2026