AccessGUDID - DEVICE: XRpad Digital X-Ray Detector System (00812589020153)

GUDID

Device Identifier (DI) Information

Brand Name: XRpad Digital X-Ray Detector System
Version or Model: XRpad IPU
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 95510922H
Company Name: PerkinElmer Technologies GmbH & Co. KG

Primary DI Number: 00812589020153
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 315030809 *Terms of Use

Device Description: Medical grade power supply with interfaces to integrate a PerkinElmer XRpad detector into an X-ray system

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?
60265	Flat panel x-ray detector integration unit	A portable, electrically-powered device intended to enable a direct flat panel detector (not included) to be integrated as part of an analogue x-ray [i.e., screen-film, computerized radiography (plate)] system to convert the analogue x-ray system into a digital x-ray system (retrofit) using the same modality components. It is typically an electronic box which is integrated into the analogue x-ray system via wired connections to each of the components (i.e., generator, exposure button, workstation and detector), whereby it synchronizes the original analogue generator with the direct flat panel detector.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
MQB	Solid State X-Ray Imager (Flat Panel/Digital Imager)

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

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
Width: 311 Millimeter
Length: 230 Millimeter
Height: 60 Millimeter

Device Record Status

Public Device Record Key: 5acf2e56-61b5-4a9a-81f6-9965fe948dff
Public Version Date: February 21, 2019
Public Version Number: 3
DI Record Publish Date: July 29, 2016