← Back to catalogue

Halyard

FDA UDI

Class II (US FDA UDI)

by Avanos Medical, Inc.

Identity

Trade Name
Halyard FDA UDI
Generic Name
Percutaneous radio-frequency ablation probe, denervation, monopolar, reusable FDA UDI
Device Name
HALYARD* Radiofrequency Probes-Steam Sterilizable-Reusable-18-54-Straight-Black-Black (Pink Stylet) FDA UDI
Model / Reference
11184 FDA UDI
Description
HALYARD* Radiofrequency Probes-Steam Sterilizable-Reusable-18-54-Straight-Black-Black (Pink Stylet) FDA UDI

Identifiers

Catalog Number
PMP-18-54 FDA UDI
Primary DI / UDI-DI
10680651111842 FDA UDI
510(k) Number
K071745 FDA UDI
FDA Product Code
GXI FDA UDI
GMDN Term
Percutaneous radio-frequency ablation probe, denervation, monopolar, reusable 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

No

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

Category: Percutaneous radio-frequency ablation probe, denervation, monopolar, reusable

Halyard 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, reusable.

Cleared under the same submission

K071745 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Avanos Medical, Inc.

Sources (1)

  • FDA UDI 4910723f-f501-495b-ba25-b48fb59bbf00 36 fields · synced Jun 9, 2026