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Avecure

FDA UDI

Class II (US FDA UDI)

by Medwaves, Inc.

Identity

Trade Name
Avecure FDA UDI
Generic Name
Microwave ablation system probe, non-powered FDA UDI
Device Name
14Gauge, Large Antenna Probe, 23cm length FDA UDI
Model / Reference
14-23-LH-4R FDA UDI
Description
14Gauge, Large Antenna Probe, 23cm length FDA UDI

Identifiers

Catalog Number
14-23-LH-4R FDA UDI
Primary DI / UDI-DI
00858584002145 FDA UDI
510(k) Number
K143203 FDA UDI
FDA Product Code
NEY FDA UDI
GMDN Term
Microwave ablation system probe, non-powered 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Category: Microwave ablation system probe, non-powered

Avecure by Medwaves, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Microwave ablation system probe, non-powered.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medwaves, Inc.

Sources (1)

  • FDA UDI 1651470a-c948-440f-a90c-2ba1f012fa73 35 fields · synced May 30, 2026