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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, single-use FDA UDI
Device Name
PMP PROBE 18G X 100MM FDA UDI
Model / Reference
98660 FDA UDI
Description
PMP PROBE 18G X 100MM FDA UDI

Identifiers

Catalog Number
PMK18100 FDA UDI
Primary DI / UDI-DI
10680651986600 FDA UDI
FDA Product Code
GXD FDA UDI
GMDN Term
Percutaneous radio-frequency ablation probe, denervation, monopolar, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4400 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

No

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, single-use

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, 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 eed7a1a3-895e-463d-8764-cf3a2c666d27 35 fields · synced Jun 9, 2026