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Neuwave

EUDAMEDFDA UDI

Class IIb (EU MDR)

Ref LN20

by NeuWave Medical, Inc.

Identity

Trade Name
NEUWAVE EUDAMEDFDA UDI
Generic Name
Microwave ablation system probe, non-powered FDA UDI
Device Name
NEUWAVE Ablation Probe EUDAMED
NEUWAVE LN Probe 20CM 17ga FDA UDI
Model / Reference
LN20 EUDAMEDFDA UDI
Description
NEUWAVE LN Probe 20CM 17ga FDA UDI

Identifiers

Catalog Number
LN20 FDA UDI
Primary DI / UDI-DI
00853719006340 EUDAMEDFDA UDI
Basic UDI-DI
081891302a0037H EUDAMED
FDA Product Code
GEI FDA UDI
EMDN Code
Z12010985 ELECTROSURGERY INSTRUMENTS - CONSUMABLES EUDAMED
GMDN Term
Microwave ablation system probe, non-powered FDA UDI

Classification

Device Class
Class IIb EUDAMED
Class II FDA UDI
Regulation Number
878.4400 FDA UDI
Market of Registration
Belgium EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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
MRI Safety
MR Unsafe FDA UDI

Category: Endoscopic electrosurgical handpiece/electrode, bipolar, single-use

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

Similar devices

Also classified as Endoscopic electrosurgical handpiece/electrode, bipolar, single-use.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
US-MF-000016783
Authorised Representative
Johnson & Johnson Medical GmbH DE-AR-000007712

Sources (2)

  • EUDAMED 337f8e7e-06b3-4714-aa3b-f1cba3a381d7 61 fields · synced Jul 12, 2026
  • FDA UDI b00d5de7-98a7-4a21-be11-c7ce4647b98a 36 fields · synced May 30, 2026