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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
Open-surgery biopsy forceps, single-use FDA UDI
Device Name
Keyes Dermal Biopsy Punch, Stainless Steel, 3mm FDA UDI
Model / Reference
033-013 FDA UDI
Description
Keyes Dermal Biopsy Punch, Stainless Steel, 3mm FDA UDI

Identifiers

Catalog Number
033-013 FDA UDI
Primary DI / UDI-DI
00840306805998 FDA UDI
FDA Product Code
LRY FDA UDI
GMDN Term
Open-surgery biopsy forceps, 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

Category: Open-surgery biopsy forceps, 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 Open-surgery biopsy forceps, 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 d7d6eccd-931a-4900-af96-e8d552598704 36 fields · synced Jun 6, 2026