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Marina Medical

FDA UDI

Class I (US FDA UDI)

by Marina Medical Instruments, Inc.

Identity

Trade Name
Marina Medical FDA UDI
Generic Name
Surgical instrument protective cap FDA UDI
Device Name
Luer Lock Cap, Non-sterile, Bag of 10 FDA UDI
Model / Reference
800-149 FDA UDI
Description
Luer Lock Cap, Non-sterile, Bag of 10 FDA UDI

Identifiers

Catalog Number
800-149 FDA UDI
Primary DI / UDI-DI
00840306809590 FDA UDI
FDA Product Code
KGZ FDA UDI
GMDN Term
Surgical instrument protective cap 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

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Surgical instrument protective cap

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

Similar devices

Also classified as Surgical instrument protective cap.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Marina Medical Instruments, Inc.

Sources (1)

  • FDA UDI a5c36fc1-1ede-4f08-8c25-2e0496191e23 35 fields · synced Jun 8, 2026