Marina Medical

FDA UDI

Class I (US FDA UDI)

by Marina Medical Instruments, Inc.

Identity

Trade Name: Marina Medical FDA UDI
Generic Name: Luer/Luer linear connector, reusable FDA UDI
Device Name: Transfer, Luer Lock to Luer Lock, ID 1.4mm FDA UDI
Model / Reference: 800-155 FDA UDI
Description: Transfer, Luer Lock to Luer Lock, ID 1.4mm FDA UDI

Identifiers

Catalog Number: 800-155 FDA UDI
Primary DI / UDI-DI: 00840306809651 FDA UDI
FDA Product Code: KGZ FDA UDI
GMDN Term: Luer/Luer linear connector, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4200 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: Luer/Luer linear connector, reusable

Marina Medical by Marina Medical Instruments, Inc. — 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: Marina Medical Instruments, Inc.

Sources (1)

FDA UDI e624670d-623a-43c2-b466-9f87c5480639 35 fields · synced Jun 6, 2026