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Medline

FDA UDI

Class II (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Medline FDA UDI
Generic Name
Air-filled bed mattress overlay FDA UDI
Device Name
PAD,MEDTECH AIR "TRUE" LOW AIR LOSS FDA UDI
Model / Reference
MDTMEDAIRPAD FDA UDI
Description
PAD,MEDTECH AIR "TRUE" LOW AIR LOSS FDA UDI

Identifiers

Catalog Number
MDTMEDAIRPAD FDA UDI
Primary DI / UDI-DI
10080196384525 FDA UDI
FDA Product Code
FNM FDA UDI
GMDN Term
Air-filled bed mattress overlay 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

Yes

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: Air-filled bed mattress overlay

Medline by Medline Industries, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Air-filled bed mattress overlay.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5e50753d-208e-49a2-a466-1a407ebf51ba 35 fields · synced May 30, 2026