Footplate Heel Cup

FDA UDI

Class I (US FDA UDI)

by Motion Concepts Inc

Identity

Trade Name: Footplate Heel Cup FDA UDI
Generic Name: Wheelchair footrest/legrest FDA UDI
Device Name: Optional Rubber Coated Footplate Heel Cups for use with MC Individual Footplate Assemblies. (Mounting hardware included) FDA UDI
Model / Reference: D-0130-0182-HC FDA UDI
Description: Optional Rubber Coated Footplate Heel Cups for use with MC Individual Footplate Assemblies. (Mounting hardware included) FDA UDI

Identifiers

Catalog Number: HC FDA UDI
Primary DI / UDI-DI: 07540147002251 FDA UDI
FDA Product Code: IMM FDA UDI
GMDN Term: Wheelchair footrest/legrest 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Wheelchair footrest/legrest

Footplate Heel Cup by Motion Concepts Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Wheelchair footrest/legrest.

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Motion Concepts Inc

Sources (1)

FDA UDI 0f980903-84c7-4548-a395-dc6e10dd473b 35 fields · synced Jun 8, 2026