Diacor CT Overlay

GUDID B237OVA30

Receiver for Brightspeed Select

Diacor, Inc.

Radiological whole-body positioner
Primary Device IDB237OVA30
NIH Device Record Key8ac9dfbf-eec4-4afb-89d8-39830f138738
Commercial Distribution StatusIn Commercial Distribution
Brand NameDiacor CT Overlay
Version Model NumberOVA-3
Company DUNS605813559
Company NameDiacor, Inc.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone801-467-0050
EmailSales@DiacorInc.com
Phone801-467-0050
EmailSales@DiacorInc.com
Phone801-467-0050
EmailSales@DiacorInc.com
Phone801-467-0050
EmailSales@DiacorInc.com
Phone801-467-0050
EmailSales@DiacorInc.com
Phone801-467-0050
EmailSales@DiacorInc.com
Phone801-467-0050
EmailSales@DiacorInc.com
Phone801-467-0050
EmailSales@DiacorInc.com
Phone801-467-0050
EmailSales@DiacorInc.com
Phone801-467-0050
EmailSales@DiacorInc.com
Phone801-467-0050
EmailSales@DiacorInc.com
Phone801-467-0050
EmailSales@DiacorInc.com
Phone801-467-0050
EmailSales@DiacorInc.com
Phone801-467-0050
EmailSales@DiacorInc.com
Phone801-467-0050
EmailSales@DiacorInc.com
Phone801-467-0050
EmailSales@DiacorInc.com
Phone801-467-0050
EmailSales@DiacorInc.com

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCB237OVA30 [Primary]

FDA Product Code

IXQTable, Radiographic, Stationary Top

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-06-16
Device Publish Date2023-06-08

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