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Wheelchair Back Cushion Foam - 22 x 19

FDA UDI

Class I (US FDA UDI)

by Compass Health Brands Corp.

Identity

Trade Name
Wheelchair Back Cushion Foam - 22 x 19 FDA UDI
Generic Name
Soft-rubber chair cushion FDA UDI
Device Name
Foam WC Back Cushion 22x19 FDA UDI
Model / Reference
BKFB-2219 FDA UDI
Description
Foam WC Back Cushion 22x19 FDA UDI

Identifiers

Primary DI / UDI-DI
00092237604335 FDA UDI
FDA Product Code
IMP FDA UDI
GMDN Term
Soft-rubber 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

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Wheelchair seat cushionSoft-rubber chair cushion

Wheelchair Back Cushion Foam - 22 x 19 by Compass Health Brands Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Soft-rubber chair cushion.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Compass Health Brands Corp.

Sources (1)

  • FDA UDI 7b325ae4-bd24-4ace-af84-69b348c8bf7b 34 fields · synced May 30, 2026