DoseLab Pro DoseLab Pro

GUDID 00861334000339

Dosimetry QA Software

VARIAN MEDICAL SYSTEMS, INC.

Accelerator system quality assurance device Accelerator system quality assurance device Accelerator system quality assurance device Accelerator system quality assurance device Accelerator system quality assurance device Accelerator system quality assurance device Accelerator system quality assurance device Accelerator system quality assurance device Accelerator system quality assurance device Accelerator system quality assurance device Accelerator system quality assurance device Accelerator system quality assurance device Accelerator system quality assurance device
Primary Device ID00861334000339
NIH Device Record Key4fb5806e-95a3-4596-9232-be2def279281
Commercial Distribution Discontinuation2019-12-31
Commercial Distribution StatusNot in Commercial Distribution
Brand NameDoseLab Pro
Version Model Number6.8.0
Catalog NumberDoseLab Pro
Company DUNS009120817
Company NameVARIAN MEDICAL SYSTEMS, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone888-263-8541
Emailsupport@mobiusmed.com
Phone888-263-8541
Emailsupport@mobiusmed.com
Phone888-263-8541
Emailsupport@mobiusmed.com
Phone888-263-8541
Emailsupport@mobiusmed.com
Phone888-263-8541
Emailsupport@mobiusmed.com
Phone888-263-8541
Emailsupport@mobiusmed.com
Phone888-263-8541
Emailsupport@mobiusmed.com
Phone888-263-8541
Emailsupport@mobiusmed.com
Phone888-263-8541
Emailsupport@mobiusmed.com
Phone888-263-8541
Emailsupport@mobiusmed.com
Phone888-263-8541
Emailsupport@mobiusmed.com
Phone888-263-8541
Emailsupport@mobiusmed.com
Phone888-263-8541
Emailsupport@mobiusmed.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100861334000339 [Primary]

FDA Product Code

IYEAccelerator, Linear, Medical

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2020-07-16
Device Publish Date2016-09-14

On-Brand Devices [DoseLab Pro]

08613340003003Dosimetry QA Software
00861334000339Dosimetry QA Software

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.