AccessGUDID - DEVICE: OneScope Pro (00860010859704)

GUDID

Device Identifier (DI) Information

Brand Name: OneScope Pro
Version or Model: OneScope Pro Video Laryngoscope
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: One-AI Healthcare, Inc

Primary DI Number: 00860010859704
Issuing Agency: GS1
Commercial Distribution End Date: December 31, 2030
Device Count: 1
Labeler D-U-N-S® Number*: 116913619 *Terms of Use

Device Description: OneScope Pro Video Laryngoscope

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?
62761	Video intubation laryngoscope handle/monitor	A non-sterile component of a bladed video intubation laryngoscope intended to enable the positioning of the blade into the oral cavity to manipulate the tongue, preventing it from obstructing the oropharynx and enabling a clear view of the trachea for the insertion of an endotracheal (ET) tube prior to the delivery of inhalation anaesthesia and/or ventilation. It has a monitor for the user to view anatomical images of the larynx/trachea transmitted by a video system from an electronic camera at the distal end of the blade. This is a reusable device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
CCW	Laryngoscope, Rigid

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: 15fca53a-d89f-4b52-b1d2-efee3190c025
Public Version Date: October 11, 2023
Public Version Number: 1
DI Record Publish Date: October 03, 2023