AccessGUDID - DEVICE: QAWeb Enterprise (05415334002432)

GUDID

Device Identifier (DI) Information

Brand Name: QAWeb Enterprise
Version or Model: V2.xx
Commercial Distribution Status: In Commercial Distribution
Catalog Number: K5402921
Company Name: Barco NV

Primary DI Number: 05415334002432
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 371618773 *Terms of Use

Device Description: QAWeb Enterprise Agent

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):	Yes
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?
64325	Radiology workstation display quality assurance software	A software application intended to be used to measure, calibrate, and adjust the display parameters of a radiology workstation monitor to standardize the quality level of digital radiological images (DICOM images) displayed by the monitor. It is typically used to manage the display quality of several computers within a healthcare facility, and to feed data (e.g., alerts) back to a central user(s). It is not intended for image processing, distribution, or viewing.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
LHO	Instrument, quality-assurance, radiologic

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: 6e091e95-ad8a-4a67-ba7c-3d48ecc7ef8d
Public Version Date: April 28, 2021
Public Version Number: 2
DI Record Publish Date: July 19, 2019

Alternative and Additional Identifiers Additional Identifiers

Package DI

[?]

Package DI Number	Quantity per Package	Contains DI Package	Package Discontinue Date	Package Status	Package Type
No Package DIs found

Secondary DI

[?]

Issuing Agency [?]	Secondary DI Number
No Secondary DIs found

Unit of Use DI

[?]

Unit of Use DI Number: No Unit of Use DI Numbers Found CLOSE

Direct Marking (DM)

[?]

Device Subject to Direct Marking (DM), but Excepted: Yes
DM DI Different from Primary DI: No
DM DI Number: None
CLOSE

Production Identifier(s) in UDI

[?]

Lot or Batch Number: No
Serial Number: No
Expiration Date: No
Manufacturing Date: No
Donation Identification Number: No CLOSE

Customer Contact

[?]

Phone: +1(866)302-7939
Email: service.medical.usa@barco.com

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