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Drivemedical

FDA UDI

Class II (US FDA UDI)

by Drive Devilbiss Healthcare

Identity

Trade Name
DRIVEMEDICAL FDA UDI
Generic Name
Alternating-pressure inflator FDA UDI
Device Name
Pressure PreventionGroup 1 Surfaces Product Description: APP Pad Only, 1/ea, RTL FDA UDI
Model / Reference
14003 FDA UDI
Description
Pressure PreventionGroup 1 Surfaces Product Description: APP Pad Only, 1/ea, RTL FDA UDI

Identifiers

Primary DI / UDI-DI
00822383103747 FDA UDI
FDA Product Code
FNM FDA UDI
GMDN Term
Alternating-pressure inflator 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Alternating-pressure bed mattress overlay systemAlternating-pressure inflatorAlternating-pressure bed mattress overlay, reusable

Drivemedical by Drive Devilbiss Healthcare — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Alternating-pressure bed mattress overlay, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Drive Devilbiss Healthcare

Sources (1)

  • FDA UDI d9ec2319-336e-4e8d-9ca8-23c5bbfa8b2f 33 fields · synced Jun 8, 2026