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Allen

FDA UDI

Class I (US FDA UDI)

by Hill-Rom, Inc.

Identity

Trade Name
ALLEN FDA UDI
Generic Name
Leg procedure positioner FDA UDI
Device Name
Adjustable Width Footboard FDA UDI
Model / Reference
900111 FDA UDI
Description
Adjustable Width Footboard FDA UDI

Identifiers

Catalog Number
O-AFB FDA UDI
Primary DI / UDI-DI
00615521019303 FDA UDI
FDA Product Code
FWZ FDA UDI
GMDN Term
Leg procedure positioner FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4950 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

Yes

FDA UDI

Category: Leg procedure positioner

Allen by Hill-Rom, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Leg procedure positioner.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hill-Rom, Inc.

Sources (1)

  • FDA UDI e476a8da-7402-48fe-8cdd-f82d46a3188d 35 fields · synced Jun 1, 2026