AccessGUDID - DEVICE: Component Monitoring System (B485CNSVID3701)

GUDID

Device Identifier (DI) Information

Brand Name: Component Monitoring System
Version or Model: CNS-VID-370
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: MOBERG RESEARCH INC

Primary DI Number: B485CNSVID3701
Issuing Agency: HIBCC
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 029957656 *Terms of Use

Device Description: International model; optional camera that can be used to record video of the patient.

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?
58857	Multi-purpose digital medical camera	An electrically-powered, hand-held digital electro-optical device designed to capture video or still image data for multiple medical applications (e.g., ophthalmoscopic, otoscopic, and dermatoscopic) using dedicated interchangeable lenses/attachments. It typically consists of a lightproof chamber with an aperture fitted with a lens and a shutter, through which the image of an object is projected onto a surface for recording. It may include a user display screen for visualization before image capture, and sometimes a docking cradle for battery recharging and connection to a personal computer.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
GWQ	Full-Montage Standard Electroencephalograph
ORT	Burst Suppression Detection Software For Electroencephalograph
MHX	Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
OMA	Amplitude-Integrated Electroencephalograph
OLT	Non-Normalizing Quantitative Electroencephalograph Software
MUD	Oximeter, Tissue Saturation

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K080217	000

Device Exempt from Premarket Submission: No 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: 764dfa41-2c96-4f5b-afd4-7d6d5f38b174
Public Version Date: November 23, 2021
Public Version Number: 2
DI Record Publish Date: October 23, 2020