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NeuroTherm™

FDA UDI

Class II (US FDA UDI)

by Neuro Therm, Inc.

Identity

Trade Name
NeuroTherm™ FDA UDI
Generic Name
Percutaneous radio-frequency ablation probe cannula, single-use FDA UDI
Device Name
Radiofrequency Cannula - Straight FDA UDI
Model / Reference
CLASSIC FDA UDI
Description
Radiofrequency Cannula - Straight FDA UDI

Identifiers

Catalog Number
S-1510-18 FDA UDI
Primary DI / UDI-DI
05415067022448 FDA UDI
FDA Product Code
GXI FDA UDI
GMDN Term
Percutaneous radio-frequency ablation probe cannula, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4725 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

Dimensions & Sizes

Size
Needle Gauge — 18 Gauge FDA UDI

Category: Percutaneous radio-frequency ablation probe cannula, single-use

NeuroTherm™ by Neuro Therm, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Percutaneous radio-frequency ablation probe cannula, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Neuro Therm, Inc.

Sources (1)

  • FDA UDI 2c0f40c4-0a50-4b60-9d54-b171e0a20009 37 fields · synced Jun 6, 2026