AccessGUDID - DEVICE: ClinicalAccess® Kiosk (00085003316723)

GUDID

Device Identifier (DI) Information

Brand Name: ClinicalAccess® Kiosk
Version or Model: 1.0
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 1CAK001
Company Name: Globalmed Holdings, LLC

Primary DI Number: 00085003316723
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 103201849 *Terms of Use

Device Description: The ClinicalAccess®, Kiosk is our most secure medical station, designed to be wall mounted or tabletop mounted, it offers all the capabilities you expect from a telemedicine station, in a small form factor. The kiosk comes equipped with 19” touchscreen, 4k conference camera, integrated small form factor PC, and lockable device storage

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?
60723	Medical image management system	A computerized image data management system designed to electronically receive, collect, store, and display a broad range of medical imaging/video data (non-dedicated), and to distribute the data within or between healthcare facilities to facilitate data analysis, organization, reporting, and sharing (e.g., teaching). The system consists of combined hardware (e.g., network switch, controller) and server/client software intended to relay image data from a broad range of imaging/audiovisual devices (e.g., endoscopic camera, ultrasound imaging system, radiography digital imaging system) to off-the-shelf devices [e.g., monitors, personal computers (PCÃ¢â‚¬â„¢s)].	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
OUG	Medical Device Data System

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: 7cf4ae45-8370-407d-9d34-9311a3187b42
Public Version Date: July 04, 2025
Public Version Number: 1
DI Record Publish Date: June 26, 2025