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Neuwave

FDA UDI

Class I (US FDA UDI)

by NeuWave Medical, Inc.

Identity

Trade Name
NEUWAVE FDA UDI
Generic Name
Microwave ablation system generator FDA UDI
Device Name
NEUWAVE Arm 2 Dovetail Rail FDA UDI
Model / Reference
ARM2 FDA UDI
Description
NEUWAVE Arm 2 Dovetail Rail FDA UDI

Identifiers

Catalog Number
ARM2 FDA UDI
Primary DI / UDI-DI
00853719006982 FDA UDI
FDA Product Code
BWN FDA UDI
GMDN Term
Microwave ablation system generator FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4950 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

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Microwave ablation system generator

Neuwave by NeuWave Medical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Microwave ablation system generator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 85cd3edc-6815-4f45-8022-91304297e7f0 36 fields · synced Jun 8, 2026