AccessGUDID - DEVICE: Prone Cart (G782MPC1000)

GUDID

Device Identifier (DI) Information

Brand Name: Prone Cart
Version or Model: MPC-100
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: Electro-Connect, Inc.

Primary DI Number: G782MPC1000
Issuing Agency: HIBCC
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 181897109 *Terms of Use

Device Description: The Prone Cart is designed for those with pressure ulcers, burns, or other injuries requiring restriction to the prone position. Designed for safety, comfort and convenience, the Prone Cart offers users independence with increased mobility. Moving throughout the hospital now becomes an option. The user-driven Prone Cart allows for upper body motion that may help build endurance and stamina.

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?
38052	Assistive wheeled stretcher	A manually-operated device designed as a wheeled stretcher with a platform made for a person with a disability in a lying position to transport themselves around. It has a flat top surface upon which the user lies on their stomach and four wheels. It is available in a variety of designs, e.g., having two large hand-propelled wheelchair type wheels at the front which also provides a steering capability, or it can be very low so that the user propels and steers by pushing directly on the floor. It will provide a person with a disability with a means of limited mobility typically without presence of an attendant.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
FPO	Stretcher, Wheeled

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: ab420ffe-01bf-4dbe-a5ec-17d0d2b20aff
Public Version Date: March 27, 2026
Public Version Number: 1
DI Record Publish Date: March 19, 2026