AccessGUDID - DEVICE: CM Legrest, Individual Calf Pad Mount (07540147002879)

GUDID

Device Identifier (DI) Information

Brand Name: CM Legrest, Individual Calf Pad Mount
Version or Model: D-0101-0157-ICPM
Commercial Distribution Status: In Commercial Distribution
Catalog Number: ICPM
Company Name: Motion Concepts Inc

Primary DI Number: 07540147002879
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 259777209 *Terms of Use

Device Description: Individual Calf Pad Mount Assy for use with the LNX Power Center Mount Legrest (upper assy) or MINI LNX Power CM Legrest (upper assy). Mounting hardware included. Standard LNX Calf Pad Mount Assy includes Independent Calf Pads (x2). Calf Pads are not included (purchased separately) with the MINI LNX Calf Pad Mount Assy.

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	No
Prescription Use (Rx):	No
Over the Counter (OTC):	No
Kit:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
32982	Wheelchair footrest/legrest	A platform (typically metal with or without a padded vinyl covering) usually mounted on a wheelchair in pairs, and upon which a wheelchair occupant may place the feet/legs for comfort, support, and/or to keep them off of the ground. It typically includes a mounting frame, footrest, and may include a mounted pad(s) to support the calves of the legs; it may be fixed or adjustable.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
KNN	Components, Wheelchair

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: Yes CLOSE

Sterilization

Device Packaged as Sterile: No
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: bbd65b8d-671b-4267-a18d-a65e671b7358
Public Version Date: October 18, 2023
Public Version Number: 3
DI Record Publish Date: December 08, 2022