AccessGUDID - DEVICE: Everest & Jennings (M36890763032A1)

GUDID

Device Identifier (DI) Information

Brand Name: Everest & Jennings
Version or Model: 90763032A
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 90763032A
Company Name: GF HEALTH PRODUCTS, INC.

Primary DI Number: M36890763032A1
Issuing Agency: HIBCC
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 132016168 *Terms of Use

Device Description: ELR PANEL&HDW BLACK-PR

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?
65005	Wheelchair legrest pad	A contoured or padded device intended to be attached to wheelchair footrests so that it can provide a comfortable platform to support the calves of the legs (legrest).	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: f02a79dc-b536-4a00-abc0-ad76796ed1f9
Public Version Date: August 12, 2021
Public Version Number: 1
DI Record Publish Date: August 04, 2021