AccessGUDID - DEVICE: Jay (00016958056785)

GUDID

Device Identifier (DI) Information

Brand Name: Jay
Version or Model: J3 Carbon Back
Commercial Distribution Status: In Commercial Distribution
Catalog Number: Jay
Company Name: SUNRISE MEDICAL (US) LLC

Primary DI Number: 00016958056785
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 962525056 *Terms of Use

Device Description: The J3 Back now offers a Carbon Fiber shell option for the ultimate in lightweight performance. Weighing as little as 2.2 lbs. when combined with RH hardware, the J3 Carbon Fiber Back is the perfect addition to any Quickie ultra lightweight wheelchair.

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):	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?
44511	Gel-filled chair cushion	A gel-filled pad designed to be placed on the seat of a chair to distribute an occupant's body weight over the surface of the buttocks, typically to relieve pressure points for comfort and to prevent pressure sores. It is commonly used for elderly immobilized patients especially in cases of decubitus ulcers, patients with disabilities, or patients with low body fat. It may be used in a wheelchair. This is a reusable device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
IMP	Cushion, 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: 96772695-2115-428c-8e08-fd0856a41c36
Public Version Date: May 20, 2025
Public Version Number: 2
DI Record Publish Date: November 10, 2023