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Drivemedical

FDA UDI

Class I (US FDA UDI)

by Drive Devilbiss Healthcare

Identity

Trade Name
DRIVEMEDICAL FDA UDI
Generic Name
Foam-filled chair cushion FDA UDI
Device Name
Pressure PreventionRetail Foam Product Description: Foam Cushion 18 x 16 x 3,1EA,12/CS FDA UDI
Model / Reference
RTL14910 FDA UDI
Description
Pressure PreventionRetail Foam Product Description: Foam Cushion 18 x 16 x 3,1EA,12/CS FDA UDI

Identifiers

Primary DI / UDI-DI
00822383247199 FDA UDI
FDA Product Code
IMP FDA UDI
GMDN Term
Foam-filled chair cushion FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3920 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Foam-filled chair cushion

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

Similar devices

Also classified as Foam-filled chair cushion.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 3311dddc-8d07-4706-8cae-16e6ec234f5d 33 fields · synced Jun 8, 2026