AccessGUDID - DEVICE: QVCAD System Installation Kit (B630QVCSIK1202346)

GUDID

Device Identifier (DI) Information

Brand Name: QVCAD System Installation Kit
Version or Model: 12.02-3.4.6
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number:
Company Name: QVIEW MEDICAL

Primary DI Number: B630QVCSIK1202346
Issuing Agency: HIBCC
Commercial Distribution End Date: January 22, 2025
Device Count: 1
Labeler D-U-N-S® Number*: 063962130 *Terms of Use
Previous DI: B630QVCSIK1010344

Device Description: Installation Kit for QVCAD System Release 3.4.6 with Debian 12.2

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?
40873	Ultrasound imaging system application software	An individual software program or group of programs, routines or algorithms that add specific image processing and/or analysis capabilities to a diagnostic ultrasound system configuration. A basic set of applications programs and routines are included with such computer-controlled imaging systems and they can be upgraded to correct programming errors or to add new system capabilities. Some applications software programs or program packages must be combined with specific hardware or firmware configurations in order to function as intended. Applications program packages are typically identified by a proprietary name and "version" or "upgrade" number.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
MYN	Analyzer, Medical Image

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
P150043	000
P150043	001

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
Handling Environment Temperature: less than 90 Degrees Fahrenheit

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: e241a160-0f22-4473-9ded-23d4aabe1ffa
Public Version Date: January 22, 2025
Public Version Number: 2
DI Record Publish Date: June 26, 2024