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Neutral Plate

FDA UDI

Class II (US FDA UDI)

by Soniquence, LLC

Identity

Trade Name
Neutral Plate FDA UDI
Generic Name
Electrosurgical return electrode, reusable FDA UDI
Device Name
Neutral plate, Flexible, Reusable, small FDA UDI
Model / Reference
SIEC-NPV FDA UDI
Description
Neutral plate, Flexible, Reusable, small FDA UDI

Identifiers

Catalog Number
SIEC-NPV FDA UDI
Primary DI / UDI-DI
00810026180934 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Electrosurgical return electrode, reusable 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

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: Electrosurgical return electrode, reusable

Neutral Plate by Soniquence, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrosurgical return electrode, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Soniquence, LLC

Sources (1)

  • FDA UDI dbba17a9-170f-441c-92f1-c8dbaac77c7c 34 fields · synced May 30, 2026