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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
Endoscope video camera FDA UDI
Device Name
Wireless Endoscopic Camera System with Wifi, 1080p, Endovision App, White FDA UDI
Model / Reference
350-525 FDA UDI
Description
Wireless Endoscopic Camera System with Wifi, 1080p, Endovision App, White FDA UDI

Identifiers

Catalog Number
350-525 FDA UDI
Primary DI / UDI-DI
00840306836374 FDA UDI
FDA Product Code
FWD FDA UDI
GMDN Term
Endoscope video camera FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4160 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

Category: Endoscope video camera

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

Similar devices

Also classified as Endoscope video camera.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI dcd49a8e-7b62-48f3-8ab1-f3300b5606da 35 fields · synced May 31, 2026