← Back to catalogue

Individual Cast Footplates

FDA UDI

Class I (US FDA UDI)

by Motion Concepts Inc

Identity

Trade Name
Individual Cast Footplates FDA UDI
Generic Name
Wheelchair footrest/legrest FDA UDI
Device Name
Individual Cast Footplate assembly (left, right or sets) for use with Motion Concepts Centermount Legrest Assemblies. (footplate sizes available in short, medium and long) FDA UDI
Model / Reference
D-0101-0157-IF FDA UDI
Description
Individual Cast Footplate assembly (left, right or sets) for use with Motion Concepts Centermount Legrest Assemblies. (footplate sizes available in short, medium and long) FDA UDI

Identifiers

Catalog Number
IF FDA UDI
Primary DI / UDI-DI
07540147002152 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

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Wheelchair footrest/legrest

Individual Cast Footplates by Motion Concepts Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wheelchair footrest/legrest.

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

Manufacturer
Motion Concepts Inc

Sources (1)

  • FDA UDI 62ec97fb-65b3-4b0a-a0e2-3787324a1357 35 fields · synced Jun 8, 2026