AccessGUDID - DEVICE: WHEELCHAIR HEADREST (00606509900034)

GUDID

Device Identifier (DI) Information

Brand Name: WHEELCHAIR HEADREST
Version or Model: WHEELCHAIR HEADREST
Commercial Distribution Status: In Commercial Distribution
Catalog Number: N/A
Company Name: Pride Mobility Products Corp

Primary DI Number: 00606509900034
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 041477449 *Terms of Use

Device Description: A padded device attached to a wheelchair, typically with a long and sturdy metal insert, to provide the wheelchair occupant with a support upon which to rest the head. The device improves user comfort and may improve some user range of vision. Its exterior is typically made of tear-resistant polyurethane. This will also include the extensions needed to attach this device.

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):	Yes
Over the Counter (OTC):	Yes
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?
41119	Wheelchair/chair/stander headrest	A padded device attached to a wheelchair, a disability-supportive chair, and/or a stander to provide a disabled patient with additional head support and comfort while in a sitting and/or standing position. This device will also include the extensions (e.g., a metal insert, screws) needed to attach this device. It may be available in various shapes and sizes, and it may be adjustable.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
IMS	Support, Head And Trunk, 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: ff1d7253-0130-43fa-8b19-29a763eda918
Public Version Date: March 05, 2024
Public Version Number: 3
DI Record Publish Date: August 26, 2019