Surgical Direct

FDA UDI

Class I (US FDA UDI)

by Surgical Direct, Inc.

Identity

Trade Name: Surgical Direct FDA UDI
Generic Name: Periosteal elevator, reusable FDA UDI
Device Name: 6 1/4 inch Duckbill Elevator, 2mm Tip FDA UDI
Model / Reference: SD914709156 FDA UDI
Description: 6 1/4 inch Duckbill Elevator, 2mm Tip FDA UDI

Identifiers

Catalog Number: SD914709156 FDA UDI
Primary DI / UDI-DI: B382SD9147091560 FDA UDI
FDA Product Code: GEG FDA UDI
GMDN Term: Periosteal elevator, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4800 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Periosteal elevator, reusable

Surgical Direct by Surgical Direct, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Periosteal elevator, reusable.

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BARRIER PLACEMENT INSTRUMENT — W.H. Holden, Inc. · Class I
ELEVATOR — KLS-Martin L.P. · Class I
HELMUT ZEPF — Helmut Zepf Medizintechnik GmbH · Class I
Ambler Surgical — Ambler Surgical, LLC · Class I

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: Surgical Direct, Inc.

Sources (1)

FDA UDI 3394c36b-963a-45f5-ae20-752b02db07c1 35 fields · synced May 31, 2026