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Matrix

FDA UDI

Class II (US FDA UDI)

by Midtown Investments, LLC

Identity

Trade Name
Matrix FDA UDI
Generic Name
Alternating-pressure bed mattress overlay, single-use FDA UDI
Device Name
Low Air Loss Mattress System, 80x36x10 FDA UDI
Model / Reference
Matrix-LALMS84 FDA UDI
Description
Low Air Loss Mattress System, 80x36x10 FDA UDI

Identifiers

Catalog Number
LALMS3684 FDA UDI
Primary DI / UDI-DI
00190885000063 FDA UDI
FDA Product Code
FNM FDA UDI
GMDN Term
Alternating-pressure bed mattress overlay, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5550 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Alternating-pressure bed mattress overlay, single-use

Matrix by Midtown Investments, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Alternating-pressure bed mattress overlay, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Midtown Investments, LLC

Sources (1)

  • FDA UDI c6cb9bd1-633d-4adc-9a19-14d27c3fa04a 34 fields · synced May 30, 2026