Marina Medical

FDA UDI

Class I (US FDA UDI)

by Marina Medical Instruments, Inc.

Identity

Trade Name: Marina Medical FDA UDI
Generic Name: General-purpose curette FDA UDI
Device Name: Kevorkian Curette Rigid, with Basket, 30cm FDA UDI
Model / Reference: 280-501 FDA UDI
Description: Kevorkian Curette Rigid, with Basket, 30cm FDA UDI

Identifiers

Catalog Number: 280-501 FDA UDI
Primary DI / UDI-DI: 00840306806742 FDA UDI
FDA Product Code: FZS FDA UDI
GMDN Term: General-purpose curette 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

MRI Safety

MR Safe FDA UDI

Category: General-purpose curette

Marina Medical by Marina Medical Instruments, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose curette.

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Ambler Surgical — Ambler Surgical, LLC · Class I
Curette — Koros USA, Inc. · Class I
BOSS Instruments — Boss Instruments, Ltd. · Class I
Millennium — AVALIGN TECHNOLOGIES, Inc. · Class I
Ambler Surgical — Ambler Surgical, LLC · Class I
Impulse Interbody Spacer System — Degen Medical · 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: Marina Medical Instruments, Inc.

Sources (1)

FDA UDI c7aaaba9-b8f0-4e5f-9844-e0861dff19b9 35 fields · synced May 30, 2026