Elmed

FDA UDI

Class I (US FDA UDI)

by Elmed Incorporated

Identity

Trade Name: ELMED FDA UDI
Generic Name: ENT elevator FDA UDI
Device Name: GOLDMAN DISPLACER AND SEPTUM ELEVATOR, 6MM WIDE TIP, 7-1/2" OVERALL LENGTH, SURGICAL GRADE AUTOCLAVABLE STAINLESS STEEL FDA UDI
Model / Reference: 42-1040TL FDA UDI
Description: GOLDMAN DISPLACER AND SEPTUM ELEVATOR, 6MM WIDE TIP, 7-1/2" OVERALL LENGTH, SURGICAL GRADE AUTOCLAVABLE STAINLESS STEEL FDA UDI

Identifiers

Catalog Number: 42-1040TL FDA UDI
Primary DI / UDI-DI: 00842180174313 FDA UDI
FDA Product Code: LRC FDA UDI
GMDN Term: ENT elevator FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 874.4420 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

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: ENT elevator

Elmed by Elmed Incorporated — Class I — 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 I	Pending data

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Manufacturer

Manufacturer: Elmed Incorporated

Sources (1)

FDA UDI a08c0351-f2a1-4b56-8621-e19ce1df1e23 35 fields · synced May 30, 2026