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Devon

FDA UDI

Class I (US FDA UDI)

by Cardinalhealth

Identity

Trade Name
Devon FDA UDI
Generic Name
Foam-filled bed mattress overlay FDA UDI
Device Name
Prone Headrest,Soft Touch FDA UDI
Model / Reference
31163184 FDA UDI
Description
Prone Headrest,Soft Touch FDA UDI

Identifiers

Catalog Number
31163184 FDA UDI
Primary DI / UDI-DI
20884527003775 FDA UDI
FDA Product Code
CCX FDA UDI
GMDN Term
Foam-filled bed mattress overlay FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.6820 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Dimensions & Sizes

Size
Outer Diameter — 7 Inch FDA UDI

Category: Foam-filled bed mattress overlay

Devon by Cardinalhealth — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Foam-filled bed mattress overlay.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinalhealth

Sources (1)

  • FDA UDI 92c4c042-4be3-4203-a73f-402b36c6f94a 37 fields · synced May 30, 2026