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AngioDynamics

FDA UDI

Class II (US FDA UDI)

by Angiodynamics, Inc

Identity

Trade Name
AngioDynamics FDA UDI
Generic Name
Percutaneous radio-frequency ablation probe, tumour-ablation, monopolar FDA UDI
Device Name
Software Module for RITA Model 1500X RF Generator FDA UDI
Model / Reference
700-104918 FDA UDI
Description
Software Module for RITA Model 1500X RF Generator FDA UDI

Identifiers

Primary DI / UDI-DI
H7877001049180 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Percutaneous radio-frequency ablation probe, tumour-ablation, monopolar 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Percutaneous radio-frequency ablation probe, tumour-ablation, monopolar

AngioDynamics by Angiodynamics, Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Percutaneous radio-frequency ablation probe, tumour-ablation, monopolar.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Angiodynamics, Inc

Sources (1)

  • FDA UDI 9d7310bf-ac19-403c-a328-77e301ec3882 34 fields · synced Oct 7, 2026