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Marina Medical

FDA UDI

Class II (US FDA UDI)

by Marina Medical Instruments, Inc.

Identity

Trade Name
Marina Medical FDA UDI
Generic Name
Endoscopic electrosurgical handpiece/electrode, monopolar, reusable FDA UDI
Device Name
Bi-Polar Bayonet Forceps, Blue Titanium Round Handle, 10mm Gold Long Area,1.0mm Tip Angled Down 45°, With Stop , 26.7cm (10.5") FDA UDI
Model / Reference
180-083NS FDA UDI
Description
Bi-Polar Bayonet Forceps, Blue Titanium Round Handle, 10mm Gold Long Area,1.0mm Tip Angled Down 45°, With Stop , 26.7cm (10.5") FDA UDI

Identifiers

Catalog Number
180-083NS FDA UDI
Primary DI / UDI-DI
00840306821455 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Endoscopic electrosurgical handpiece/electrode, monopolar, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4400 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 — 26.7 Centimeter FDA UDI

Category: Endoscopic electrosurgical handpiece/electrode, monopolar, reusable

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

Similar devices

Also classified as Endoscopic electrosurgical handpiece/electrode, monopolar, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6ec7374d-b2a4-40f4-909e-a072f6f56d36 36 fields · synced Jun 1, 2026