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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
General-purpose light source FDA UDI
Device Name
Light Source 50w LED 4 Port turret, w/US power Cord FDA UDI
Model / Reference
250-807 FDA UDI
Description
Light Source 50w LED 4 Port turret, w/US power Cord FDA UDI

Identifiers

Catalog Number
250-807 FDA UDI
Primary DI / UDI-DI
00840306830990 FDA UDI
FDA Product Code
EQH FDA UDI
GMDN Term
General-purpose light source FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.4350 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

Dimensions & Sizes

Size
Length — 4.25 Centimeter FDA UDI

Category: General-purpose light source

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 light source.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6e837779-c8f4-48e6-8e00-95b5afd7e92d 36 fields · synced Jun 1, 2026