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Radiofrequency Single-Use Probe

FDA UDI

Class II (US FDA UDI)

by Avanos Medical, Inc.

Identity

Trade Name
Radiofrequency Single-Use Probe FDA UDI
Generic Name
Percutaneous radio-frequency ablation probe, denervation, monopolar, single-use FDA UDI
Device Name
RF Probe, Straight - Single Use FDA UDI
Model / Reference
PMP-21-50-SU FDA UDI
Description
RF Probe, Straight - Single Use FDA UDI

Identifiers

Catalog Number
PMP-21-50-SU FDA UDI
Primary DI / UDI-DI
00193493124930 FDA UDI
FDA Product Code
GXI FDA UDI
GMDN Term
Percutaneous radio-frequency ablation probe, denervation, monopolar, 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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Percutaneous radio-frequency ablation probe, denervation, monopolar, single-use

Radiofrequency Single-Use Probe by Avanos Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Avanos Medical, Inc.

Sources (1)

  • FDA UDI 21cc7ff2-bac2-4c03-9dfe-ebee0566b0ed 35 fields · synced Jun 9, 2026