Mobius3D Mobius3D

GUDID 00861334000315

Secondary Check 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 ID00861334000315
NIH Device Record Key93859f87-47a0-480b-923e-ca418b280561
Commercial Distribution Discontinuation2019-12-31
Commercial Distribution StatusNot in Commercial Distribution
Brand NameMobius3D
Version Model Number2.0.1
Catalog NumberMobius3D
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
GS100861334000315 [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 [Mobius3D]

08613340003001Secondary Check QA Software
00861334000315Secondary Check QA Software
008508000060434.0

Trademark Results [Mobius3D]

Mark Image

Registration | Serial
Company
Trademark
Application Date
MOBIUS3D
MOBIUS3D
86175648 5188939 Live/Registered
Mobius Medical Systems, LP
2014-01-27
MOBIUS3D
MOBIUS3D
76533741 not registered Dead/Abandoned
Oregon3D, Inc.
2003-07-21

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