DynaRest Foam Mattress

FDA UDI

Class I (US FDA UDI)

by Dynarex Corp.

Identity

Trade Name: DynaRest Foam Mattress FDA UDI
Generic Name: Foam bed mattress FDA UDI
Device Name: DynaRest Multi-Zone Foam Pressure Mattress with perimeter 36"x 80" 1pc/cs FDA UDI
Model / Reference: 10420P FDA UDI
Description: DynaRest Multi-Zone Foam Pressure Mattress with perimeter 36"x 80" 1pc/cs FDA UDI

Identifiers

Primary DI / UDI-DI: 00616784042022 FDA UDI
FDA Product Code: IKY FDA UDI
GMDN Term: Foam bed mattress FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 880.5150 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

Yes

FDA UDI

Category: Foam bed mattress

DynaRest Foam Mattress by Dynarex Corp. — 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: Dynarex Corp.

Sources (1)

FDA UDI faf75392-c298-4d2f-bb4a-1e13ec5cdaa2 33 fields · synced May 31, 2026