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PrevaMatt

FDA UDI

Class I (US FDA UDI)

by Joerns Healthcare

Identity

Trade Name
PrevaMatt FDA UDI
Generic Name
Foam bed mattress FDA UDI
Device Name
253-4276 FDA UDI
Model / Reference
253-4276 FDA UDI
Description
253-4276 FDA UDI

Identifiers

Primary DI / UDI-DI
00810055884148 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

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Foam bed mattress

PrevaMatt by Joerns Healthcare — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Foam bed mattress.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Joerns Healthcare

Sources (1)

  • FDA UDI 07671f9b-de18-4235-bc08-9c1cbcb74b2a 33 fields · synced Jun 9, 2026