← Back to catalogue

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
Bayonet, Monopolar Hand Switching Forceps with 1mm non-stick tips and 3 prong plug, 25.4cm (10") FDA UDI
Model / Reference
180-110NS FDA UDI
Description
Bayonet, Monopolar Hand Switching Forceps with 1mm non-stick tips and 3 prong plug, 25.4cm (10") FDA UDI

Identifiers

Catalog Number
180-110NS FDA UDI
Primary DI / UDI-DI
00840306821530 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 — 25.4 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 36eae8b0-557a-4212-aed5-c56c56895e16 36 fields · synced Jun 8, 2026