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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
Wire/ligature passer, reusable FDA UDI
Device Name
Marina Fascia Stripper, 1cm I.D., Inner Stripper FDA UDI
Model / Reference
350-400 FDA UDI
Description
Marina Fascia Stripper, 1cm I.D., Inner Stripper FDA UDI

Identifiers

Catalog Number
350-400 FDA UDI
Primary DI / UDI-DI
00840306830266 FDA UDI
FDA Product Code
HCF FDA UDI
GMDN Term
Wire/ligature passer, reusable 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

Dimensions & Sizes

Size
Length — 1 Centimeter FDA UDI

Category: Wire/ligature passer, reusable

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

Similar devices

Also classified as Wire/ligature passer, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d68d819b-860d-484f-bd93-228f7b69c8ef 36 fields · synced Jun 6, 2026