Marina Medical

FDA UDI

Class I (US FDA UDI)

by Marina Medical Instruments, Inc.

Identity

Trade Name: Marina Medical FDA UDI
Generic Name: General-purpose bowl, reusable FDA UDI
Device Name: Sponge Bowl, Stainless Steel: 16.5 cm x 7.5 cm / 38 oz. FDA UDI
Model / Reference: 020-072 FDA UDI
Description: Sponge Bowl, Stainless Steel: 16.5 cm x 7.5 cm / 38 oz. FDA UDI

Identifiers

Catalog Number: 020-072 FDA UDI
Primary DI / UDI-DI: 00840306800054 FDA UDI
FDA Product Code: MDM FDA UDI
GMDN Term: General-purpose bowl, 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

MRI Safety

MR Safe FDA UDI

Category: General-purpose bowl, reusable

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

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Marina Medical Instruments, Inc.

Sources (1)

FDA UDI c39b00ea-c208-4c29-955d-247ee0e9a867 35 fields · synced May 31, 2026