AccessGUDID - DEVICE: Jay X2 (00016958056716)

GUDID

Device Identifier (DI) Information

Brand Name: Jay X2
Version or Model: X2
Commercial Distribution Status: In Commercial Distribution
Catalog Number: E2622
Company Name: SUNRISE MEDICAL (US) LLC

Primary DI Number: 00016958056716
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 962525056 *Terms of Use

Device Description: The JAY X2® is a lightweight, maintenance-free, fluid wheelchair cushion with a reduced profile that is designed to provide stability and pressure relief to active clients. Using elements from the JAY Xtreme and Active cushions, the X2 combines JAY’s time-tested designs with its latest technologies.

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":	Yes
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: af63b9f9-582f-4c33-97cc-ff9d8e8a3caf
Public Version Date: May 20, 2025
Public Version Number: 2
DI Record Publish Date: September 05, 2023