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MicroThermX Microwave Ablation System

FDA UDI

Class II (US FDA UDI)

by Perseon Corporation

Identity

Trade Name
MicroThermX Microwave Ablation System FDA UDI
Generic Name
Microwave ablation system generator FDA UDI
Device Name
MicroThermX Microwave Ablation System - Tabletop Stand FDA UDI
Model / Reference
MTX-180-T2 FDA UDI
Description
MicroThermX Microwave Ablation System - Tabletop Stand FDA UDI

Identifiers

Catalog Number
MTX-180-T2 FDA UDI
Primary DI / UDI-DI
00851551005019 FDA UDI
510(k) Number
K141785 FDA UDI
FDA Product Code
NEY FDA UDI
GMDN Term
Microwave ablation system generator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4400 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Microwave ablation system generator

MicroThermX Microwave Ablation System by Perseon Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Microwave ablation system generator.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Perseon Corporation

Sources (1)

  • FDA UDI 285ed653-c615-43e7-9c3f-c462860764f5 37 fields · synced May 30, 2026