Electrosurgical Unit MCB

FDA UDI

Class II (US FDA UDI)

by Lamidey Noury Medical

Identity

Trade Name: Electrosurgical Unit MCB FDA UDI
Generic Name: Electrosurgical system generator FDA UDI
Model / Reference: V10GMCBUS FDA UDI

Identifiers

Catalog Number: V10GMCBUS FDA UDI
Primary DI / UDI-DI: 03665415002116 FDA UDI
510(k) Number: K222542 FDA UDI
FDA Product Code: GEI FDA UDI
KNS FDA UDI
GMDN Term: Electrosurgical system generator FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 878.4400 FDA UDI
876.4300 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

MRI Safety

MR Unsafe FDA UDI

Category: Electrosurgical system generator

Electrosurgical Unit MCB by Lamidey Noury Medical — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Lamidey Noury Medical

Sources (1)

FDA UDI c95147fd-884b-44f6-bb7f-08b3e746bd1c 35 fields · synced May 30, 2026