← Back to catalogue

Inspired

FDA UDI

Class I (US FDA UDI)

by Drive Devilbiss Healthcare

Identity

Trade Name
INSPIRED FDA UDI
Generic Name
Foam-filled chair cushion FDA UDI
Device Name
InspiredActivity Positioning Product Description: P Pod Mobilty Base, L FDA UDI
Model / Reference
APP-A9002L FDA UDI
Description
InspiredActivity Positioning Product Description: P Pod Mobilty Base, L FDA UDI

Identifiers

Primary DI / UDI-DI
00822383939049 FDA UDI
FDA Product Code
PRN FDA UDI
GMDN Term
Foam-filled chair cushion FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5680 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-filled chair cushion

Inspired 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI f1acfc0f-bdf2-48f1-835a-d93912e15ea6 33 fields · synced Jun 8, 2026