← Back to catalogue

Marina Medical

FDA UDI

Class I (US FDA UDI)

by Marina Medical Instruments, Inc.

Identity

Trade Name
Marina Medical FDA UDI
Generic Name
Orthopaedic bone pin sharpener FDA UDI
Device Name
Dual soft/hard Stone Sharpener (2 Sizes) FDA UDI
Model / Reference
200-801 FDA UDI
Description
Dual soft/hard Stone Sharpener (2 Sizes) FDA UDI

Identifiers

Catalog Number
200-801 FDA UDI
Primary DI / UDI-DI
00840306823626 FDA UDI
FDA Product Code
EMI FDA UDI
GMDN Term
Orthopaedic bone pin sharpener FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 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: Orthopaedic bone pin sharpener

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

Similar devices

Also classified as Orthopaedic bone pin sharpener.

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

Manufacturer
Marina Medical Instruments, Inc.

Sources (1)

  • FDA UDI f38b296c-7b8b-4431-a930-cd6eedf9fcc5 35 fields · synced May 30, 2026