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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 soft-tissue manipulation forceps, tweezers-like, single-use FDA UDI
Device Name
Tissue Forceps, 1x2, Smooth, 20 cm FDA UDI
Model / Reference
060-048 FDA UDI
Description
Tissue Forceps, 1x2, Smooth, 20 cm FDA UDI

Identifiers

Catalog Number
060-048 FDA UDI
Primary DI / UDI-DI
00840306801310 FDA UDI
FDA Product Code
HTD FDA UDI
GMDN Term
Surgical soft-tissue manipulation forceps, tweezers-like, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

Dimensions & Sizes

Size
Length — 20 Centimeter FDA UDI

Category: Surgical soft-tissue manipulation forceps, tweezers-like, single-use

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 soft-tissue manipulation forceps, tweezers-like, single-use.

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 8bd2f8b5-e50e-42ac-ab62-633c36e48dfa 36 fields · synced Jun 1, 2026